NODU KANDAI 野津寛大

… Alternative Names

KANDAI Nozu 野津寛大

NOZU Kandai 野津寛大

野津寛大ノヅカンダイ

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Researcher Number	70362796
Other IDs
External Links
Affiliation (Current)	2025: 神戸大学, 医学研究科, 教授
Affiliation (based on the past Project Information) *help	2020 – 2024: 神戸大学, 医学研究科, 教授 2018 – 2020: 神戸大学, 医学研究科, 特命教授 2017: 神戸大学, 医学部附属病院, 准教授 2017: 神戸大学, 医学部附属病院, 助教 2017: 神戸大学, 大学院医学研究科内科系講座小児化学分野, 准教授 … More 2016 – 2017: 神戸大学, 医学研究科, 准教授 2016: 神戸大学, 医学(系)研究科(研究院), 准教授 2013 – 2015: 神戸大学, 医学部附属病院, 講師 2009 – 2010: Kobe University, 医学部附属病院, 助教 2007 – 2008: Kobe University, 医学部・附属病院, 助教 2005 – 2006: 神戸大学, 医学部附属病院, 助手 2003: 神戸大学, 大学院・医学系研究科, 助手 Less
Review Section/Research Field	Principal Investigator Pediatrics / Basic Section 53040:Nephrology-related Except Principal Investigator Kidney internal medicine / Basic Section 52050:Embryonic medicine and pediatrics-related / Basic Section 53040:Nephrology-related / Medium-sized Section 53:Organ-based internal medicine and related fields / Pediatrics / Embryonic/Neonatal medicine
Keywords	Principal Investigator ギッテルマン症候群 / 核酸医薬 / エクソンスキッピング / Gitelman症候群 / Bartter症候群 / 遺伝子解析 / バーター症候群 / チャネル・トランスポーター / 尿細管機能障害 / ファブリー病 … More / アルポート症候群 / スプライシング / アンチセンス治療薬 / RNA sequence / minigene / アンチセンスオリゴ / splicing / 嚢胞性線維症 / 遺伝性クロル下痢症 / 遺伝性高カルシウム尿性低カルシウム血症 / ターゲットシークエンス / 遺伝性塩類喪失性尿細管機能異常症 / 遺伝性低マグネシウム血症 / Copy number variation / 次世代シークエンサー / 遺伝性尿細管機能異常症 / 塩類喪失性尿細管機能異常症 / 小児腎臓病学 / ナンセンスリードスルー / ナンセンスリードスルー療法 / 遺伝性腎疾患 / 尿細管異常 / 先天性腎疾患 / 遺伝子 / バーター症候 / 尿中落下細胞 / トランスポーター / イオンチャネル … More Except Principal Investigator 小児ネフローゼ症候群 / ネフローゼ症候群 / 抗ネフリン抗体 / ネフリン / 疾患感受性遺伝子 / 腎臓学 / エクソンスキッピング / アルポート症候群 / PI(4,5)P2 / Dent disease-2 / Lowe症候群 / OCRL / レニン・アンギオテンシン・アルドステロン系 / 早産、低出生体重児 / リツキシマブ / GWASメタ解析 / 腎臓オルガノイド / iPS細胞 / 器官システム内科学 / フィンランド型先天性ネフローゼ症候群 / ゲノムワイド関連解析 / ステロイド感受性ネフローゼ症候群 / 診断 / 修飾遺伝子 / 高い診断能力 / 体細胞モザイク / 網羅的遺伝子解析 / 次世代シークエンサー / Alport症候群 / 重症化機序 / Malaysian / TATA-box / G493R mutation / G71R mutation / the UGT1A1 gene / Gilbert syndrome / neonatal jaundice / DHPLCスクリーニング / マレー・マレーシア人 / ジャワ・インドネシア人 / UGT1 A1遺伝子 / マレーシア人 / TATA box / G493R変異 / G71R変異 / UGT1A1遺伝子 / Gilbert症候群 / 新生児黄疸 / 遺伝子 / 医療・福祉 / アンチセンスオリゴヌクレオチド / 分子治療 / 多嚢胞性異形成腎(MCDK) / TCF2 / genome-wide CNV array / copy number variation(CNV) / microduplication / microdeletion / copy number variation (CNV) / 先天性腎尿路奇形(CAKUT) / 原因遺伝子 / CNV解析 / 先天性腎尿路奇形 Less

Elucidation of the mechanism of rituximab-induced long-term remission in childhood nephrotic syndrome
- Principal Investigator
  
  飯島一誠
- Project Period (FY)
  2023 – 2025
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 53040:Nephrology-related
- Research Institution
  Kobe University
レニンアンギオテンシン系に着目した早産、低出生体重児の腎障害進展機序の解明研究
- Principal Investigator
  
  石森真吾
- Project Period (FY)
  2023 – 2025
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Aijinkai Healthcare Corporation Takatsuki General Hospital Clinical Research Center
OCRL異常の病態解明とLowe症候群に対する酵素補充療法の開発
- Principal Investigator
  
  榊原菜々
- Project Period (FY)
  2023 – 2025
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 52050:Embryonic medicine and pediatrics-related
- Research Institution
  Kobe University
Contribution of aberrant splicing to the onset mechanisms in inherited kidney diseasesPrincipal Investigator
- Principal Investigator
  
  野津寛大
- Project Period (FY)
  2023 – 2025
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 53040:Nephrology-related
- Research Institution
  Kobe University
Joint international Research Project for International GWAS Meta-Analysis and Anti-Nephrin Autoantibodies in Childhood Nephrotic Syndrome
- Principal Investigator
  
  Iijima Kazumoto
- Project Period (FY)
  2021 – 2023
- Research Category
  
  Fund for the Promotion of Joint International Research (Fostering Joint International Research (B))
- Review Section
  
  Medium-sized Section 53:Organ-based internal medicine and related fields
- Research Institution
  Kobe University
Clarification of the pathogenesis of childhood nephrotic syndrome using iPS cell-derived kidney organoids
- Principal Investigator
  
  Iijima Kazumoto
- Project Period (FY)
  2020 – 2022
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Review Section
  
  Basic Section 53040:Nephrology-related
- Research Institution
  Kobe University
Contribution of aberrant splicing to the onset mechanisms in inherited kidney diseasesPrincipal Investigator
- Principal Investigator
  
  Kandai Nozu
- Project Period (FY)
  2019 – 2021
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Review Section
  
  Basic Section 53040:Nephrology-related
- Research Institution
  Kobe University
Joint International Research for identification of disease-susceptible genes and drug-sensitive genes in childhood nephrotic syndrome
- Principal Investigator
  
  IIJIMA KAZUMOTO
- Project Period (FY)
  2018 – 2020
- Research Category
  
  Fund for the Promotion of Joint International Research (Fostering Joint International Research (B))
- Review Section
  
  Medium-sized Section 53:Organ-based internal medicine and related fields
- Research Institution
  Kobe University
Identification of Genes Involved in the Severity of Alport Syndrome and Elucidation of the Mechanism of its Severity
- Principal Investigator
  
  Iijima Kazumoto
- Project Period (FY)
  2017 – 2019
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Kidney internal medicine
- Research Institution
  Kobe University
Establishment of a comprehensive diagnostic method using next generation sequencer for Alport syndrome
- Principal Investigator
  
  Yamamura Tomohiko
- Project Period (FY)
  2016 – 2017
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Pediatrics
- Research Institution
  Kobe University
The onset mechanisms for inherited salt-losing tubulopathiesPrincipal Investigator
- Principal Investigator
  
  Nozu Kandai
- Project Period (FY)
  2015 – 2017
- Research Category
  
  Grant-in-Aid for Scientific Research (C)
- Research Field
  
  Pediatrics
- Research Institution
  Kobe University
Development of molecular therapy for Alport syndrome
- Principal Investigator
  
  Iijima Kazumoto
- Project Period (FY)
  2014 – 2017
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Kidney internal medicine
- Research Institution
  Kobe University
Nonsense read-through therapy for Aport syndromePrincipal Investigator
- Principal Investigator
  
  KANDAI Nozu
- Project Period (FY)
  2013 – 2014
- Research Category
  
  Grant-in-Aid for Research Activity Start-up
- Research Field
  
  Pediatrics
- Research Institution
  Kobe University
最新の遺伝子解析技術を駆使した先天性尿細管チャネル・輸送体異常症の分子機構の解明Principal Investigator
- Principal Investigator
  
  野津寛大
- Project Period (FY)
  2009 – 2010
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Pediatrics
- Research Institution
  Kobe University
Identification of novel genes for congenital anomalies of Kidney and urinary tract (CAKUT) by CNV analyses and development of comprehensive gene testing for CAKUT
- Principal Investigator
  
  IIJIMA Kazumoto
- Project Period (FY)
  2008 – 2010
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Kidney internal medicine
- Research Institution
  Kobe University
Molecular analysis for inherited tubulopathiesPrincipal Investigator
- Principal Investigator
  
  NOZU Kandai
- Project Period (FY)
  2007 – 2008
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Pediatrics
- Research Institution
  Kobe University
尿細管上皮イオンチヤンネル・トランスポーター異常症の分子機構に関する研究Principal Investigator
- Principal Investigator
  
  野津寛大
- Project Period (FY)
  2005 – 2006
- Research Category
  
  Grant-in-Aid for Young Scientists (B)
- Research Field
  
  Pediatrics
- Research Institution
  Kobe University
Molecular epidemiology of neonatal Gilbert's syndrome in Malaysia
- Principal Investigator
  
  NISHIO Hisahide
- Project Period (FY)
  2003 – 2004
- Research Category
  
  Grant-in-Aid for Scientific Research (B)
- Research Field
  
  Embryonic/Neonatal medicine
- Research Institution
  Kobe University

[Book] 12.Bartter症候群、Gitelman症候群2015
- Author(s)
  野津寛大
- Total Pages
  629
- Publisher
  医学書院
- Data Source
  KAKENHI-PROJECT-15K09691
[Book] Alport症候群の軽症亜型　Annual Review 2015腎臓2015
- Author(s)
  野津寛大、飯島一誠
- Total Pages
  230
- Publisher
  中外医学社
- Data Source
  KAKENHI-PROJECT-26293203
[Book] Annual Review腎臓2010小児科領域TCF2遺伝子異常と先天性腎尿路奇形.(御手洗哲也, 東原英二, 秋澤忠男, 五十嵐隆, 金井好克編)2010
- Author(s)
  中山真紀子, 野津寛大, 飯島一誠
- Publisher
  中外医学社
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] 【腎臓学この1年の進歩】ネフリンとネフローゼ症候群2024
- Author(s)
  飯島一誠, 堀之内智子, 長野智那, 野津寛大
- Journal Title
  
  日本腎臓学会誌
  
  Volume: 66巻 Pages: 303-309
- Data Source
  KAKENHI-PROJECT-21KK0147
[Journal Article] Role of Iron in Children With Immunoglobulin A Nephropathy and Macrohematuria-Induced Acute Kidney Injury2024
- Author(s)
  Ishimori Shingo、Horinouchi Tomoko、Yamamura Tomohiko、Fujimura Junya、Kamiyoshi Naohiro、Kaito Hiroshi、Tanaka Yuriko、Matsukura Hiroyoshi、Shimabukuro Wataru、Shima Yuko、Kawaguchi Azusa、Araki Yoshinori、Nakanishi Koichi、Hara Shigeo、Nozu Kandai
- Journal Title
  
  Kidney International Reports
  
  Volume: 未 Issue: 6 Pages: 1664-1673
- DOI
  10.1016/j.ekir.2024.03.003
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-23K07242
[Journal Article] 【遺伝を考える】(II章)遺伝学的診断　個別診療分野における遺伝学的診断の進歩　腎・泌尿器領域2023
- Author(s)
  飯島一誠, 堀之内智子, 野津寛大
- Journal Title
  
  日本医師会雑誌
  
  Volume: 152巻特別1
- Data Source
  KAKENHI-PROJECT-21KK0147
[Journal Article] Rituximab in combination with cyclosporine and steroid pulse therapy for childhood-onset multidrug-resistant nephrotic syndrome: a multicenter single-arm clinical trial (JSKDC11 trial)2023
- Author(s)
  Nozu Kandai、Sako Mayumi、Tanaka Seiji、Kano Yuji、Ohwada Yoko、Morohashi Tamaki、Hamada Riku、Ohtsuka Yasufumi、Oka Masafumi、Kamei Koichi、Inaba Aya、Ito Shuichi、Sakai Tomoyuki、Kaito Hiroshi、Shima Yuko et al.
- Journal Title
  
  Clinical and Experimental Nephrology
  
  Volume: 28 Issue: 4 Pages: 337-348
- DOI
  10.1007/s10157-023-02431-0
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-23K07300, KAKENHI-PROJECT-21KK0147, KAKENHI-PROJECT-23K27617
[Journal Article] 【遺伝を考える】(II章)遺伝学的診断　個別診療分野における遺伝学的診断の進歩　腎・泌尿器領域2023
- Author(s)
  飯島一誠, 堀之内智子, 野津寛大
- Journal Title
  
  日本医師会雑誌
  
  Volume: 152巻特別1
- Data Source
  KAKENHI-PROJECT-23K27617
[Journal Article] Systematic Review of Clinical Characteristics and Genotype-Phenotype Correlation in LAMB2-Associated Disease2023
- Author(s)
  Suzuki Ryota、Sakakibara Nana、Ichikawa Yuta、Kitakado Hideaki、Ueda Chika、Tanaka Yu、Okada Eri、Kondo Atsushi、Ishiko Shinya、Ishimori Shingo、Nagano China、Yamamura Tomohiko、Horinouchi Tomoko、Okamoto Takayuki、Nozu Kandai
- Journal Title
  
  Kidney International Reports
  
  Volume: 8 Issue: 9 Pages: 1811-1821
- DOI
  10.1016/j.ekir.2023.06.019
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-23K07698
[Journal Article] A multicenter retrospective study of calcineurin inhibitors in nephrotic syndrome secondary to podocyte gene variants2023
- Author(s)
  Malakasioti G, Iancu D, Milovanova A, Tsygin A, Horinouchi T, Nagano C, Nozu K, Kamei K, Fujinaga S, Iijima K, et al. ; CNI in Monogenic SRNS Study Investigators
- Journal Title
  
  Kidney International
  
  Volume: 103 Issue: 5 Pages: 962-972
- DOI
  10.1016/j.kint.2023.02.022
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21KK0147, KAKENHI-PROJECT-20H03698
[Journal Article] All reported non-canonical splice site variants in GLA cause aberrant splicing2023
- Author(s)
  Okada Eri、Horinouchi Tomoko、Yamamura Tomohiko、Aoto Yuya、Suzuki Ryota、Ichikawa Yuta、Tanaka Yu、Masuda Chika、Kitakado Hideaki、Kondo Atsushi、Sakakibara Nana、Ishiko Shinya、Nagano China、Ishimori Shingo、Usui Joichi、Yamagata Kunihiro、Matsuo Masafumi、Nozu Kandai
- Journal Title
  
  Clinical and Experimental Nephrology
  
  Volume: 27 Issue: 9 Pages: 737-746
- DOI
  10.1007/s10157-023-02361-x
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-23K18308, KAKENHI-PROJECT-23K07698, KAKENHI-PROJECT-23K21401
[Journal Article] Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome2023
- Author(s)
  Barry A, McNulty MT, Jia X, Nagano C, Horinouchi T, Nozu K, Tokunaga K, Ronco P, Iijima K, Sampson MG, et al.
- Journal Title
  
  Nature Communications
  
  Volume: 14 Issue: 1 Pages: 2481-2481
- DOI
  10.1038/s41467-023-37985-w
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-21KK0147, KAKENHI-PROJECT-23K27617
[Journal Article] Clinical features of autosomal recessive polycystic kidney disease in the Japanese population and analysis of splicing in PKHD1 gene for determination of phenotypes2022
- Author(s)
  Ishiko S, Morisada N, Kondo A, Nagai S, Aoto Y, Okada E, Rossanti R, Sakakibara N, Nagano C, Horinouchi T, Yamamura T, Ninchoji T, Kaito H, Hamada R, Shima Y, Nakanishi K, Matsuo M, Iijima K, Nozu K.
- Journal Title
  
  Clin Exp Nephrol .
  
  Volume: 26 Issue: 2 Pages: 140-153
- DOI
  10.1007/s10157-021-02135-3
- NAID
  120007188940
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07799, KAKENHI-PROJECT-19K08726
[Journal Article] Clinical, Pathological, and Genetic Characteristics in Patients with Focal Segmental Glomerulosclerosis2022
- Author(s)
  Nagano C, Hara S, Yoshikawa N, Takeda A, Gotoh Y, Hamada R, Matsuoka K, Yamamoto M, Fujinaga S, Sakuraya K, Kamei K, Hamasaki Y, Oguchi H, Araki Y, Ogawa Y, Okamoto T, Ito S, Tanaka S, Kaito H, Aoto Y, Ishiko S, Rossanti R, Sakakibara N, Horinouchi T, Yamamura T, Nagase H, Iijima K, Nozu K
- Journal Title
  
  Kidney360
  
  Volume: 3 Issue: 8 Pages: 1384-1393
- DOI
  10.34067/kid.0000812022
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-21KK0147, KAKENHI-PROJECT-20H03698
[Journal Article] The Contribution of COL4A5 Splicing Variants to the Pathogenesis of X-Linked Alport Syndrome2022
- Author(s)
  Yamamura Tomohiko、Horinouchi Tomoko、Aoto Yuya、Lennon Rachel、Nozu Kandai
- Journal Title
  
  Frontiers in Medicine
  
  Volume: 9
- DOI
  10.3389/fmed.2022.841391
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K08726
[Journal Article] An updated view of the pathogenesis of steroid-sensitive nephrotic syndrome2022
- Author(s)
  Horinouchi Tomoko、Nozu Kandai、Iijima Kazumoto
- Journal Title
  
  Pediatric Nephrology
  
  Volume: - Issue: 9 Pages: 1957-1965
- DOI
  10.1007/s00467-021-05401-4
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-20H03698, KAKENHI-PROJECT-20K16892, KAKENHI-PROJECT-21KK0147
[Journal Article] Is influenza vaccination associated with nephrotic syndrome relapse in children? A multicenter prospective study2022
- Author(s)
  Ishimori S, Horinouchi T, Fujimura J, Yamamura T, Matsunoshita N, Kamiyoshi N, Sato M, Ogura M, Kamei K, Ishikura K, Iijima K, Nozu K
- Journal Title
  
  Pediatric Nephrology
  
  Volume: Nov 30 Issue: 7 Pages: 2107-2116
- DOI
  10.1007/s00467-022-05783-z
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21KK0147, KAKENHI-PROJECT-20H03698
[Journal Article] Utility of glomerular Gd-IgA1 staining for indistinguishable cases of IgA nephropathy or Alport syndrome2021
- Author(s)
  Ishiko Shinya、Tanaka Akihito、Takeda Asami、Hara Masayuki、Hamano Naoto、Koizumi Masahiro、Ueno Toshinori、Hayashi Hiroki、Kondo Atsushi、Nagai Sadayuki、Aoto Yuya、Nozu Kandai
- Journal Title
  
  Clinical and Experimental Nephrology
  
  Volume: Epub Issue: 7 Pages: 779-787
- DOI
  10.1007/s10157-021-02054-3
- NAID
  120007125745
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K08726, KAKENHI-PROJECT-20K17295, KAKENHI-PROJECT-18K07799
[Journal Article] Usefulness of functional splicing analysis to confirm precise disease pathogenesis in Diamond-Blackfan anemia caused by intronic variants in <i>RPS19</i>2021
- Author(s)
  Takafuji Satoru、Mori Takeshi、Nishimura Noriyuki、Yamamoto Nobuyuki、Uemura Suguru、Nozu Kandai、Terui Kiminori、Toki Tsutomu、Ito Etsuro、Muramatsu Hideki、Takahashi Yoshiyuki、Matsuo Masafumi、Yamamura Tomohiko、Iijima Kazumoto
- Journal Title
  
  Pediatric Hematology and Oncology
  
  Volume: 38 Issue: 6 Pages: 515-527
- DOI
  10.1080/08880018.2021.1887984
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K08726, KAKENHI-PROJECT-23K21429
[Journal Article] Clear Evidence of <i>LAMA5</i> Gene Biallelic Truncating Variants Causing Infantile Nephrotic Syndrome2021
- Author(s)
  Taniguchi Yukimasa、Nagano China、Sekiguchi Kiyotoshi、Tashiro Atsushi、Sugawara Noriko、Sakaguchi Haruhide、Umeda Chisato、Aoto Yuya、Ishiko Shinya、Rossanti Rini、Sakakibara Nana、Horinouchi Tomoko、Yamamura Tomohiko、Kondo Atsushi、Nagai Sadayuki、Nagase Hiroaki、Iijima Kazumoto、Miner Jeffrey H.、Nozu Kandai
- Journal Title
  
  Kidney360
  
  Volume: 2 Issue: 12 Pages: 1968-1978
- DOI
  10.34067/kid.0004952021
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K08726, KAKENHI-PROJECT-20K16892
[Journal Article] An extremely mild clinical course in a case with LAMB2-associated nephritis diagnosed with next-generation sequencing.2021
- Author(s)
  Sakuraya K, Nozu K, Murakami H, Nagano C, Horinouchi T, Fujinaga S, Iijima K, Ohtomo Y.
- Journal Title
  
  CEN Case Reports
  
  Volume: - Issue: 3 Pages: 359-363
- DOI
  10.1007/s13730-021-00574-1
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18KK0244, KAKENHI-PROJECT-19K08726
[Journal Article] A disease-causing variant of COL4A5 in a Chinese family with Alport syndrome: a case series2021
- Author(s)
  Wu Jing、Zhang Jun、Liu Li、Zhang Bo、Yamamura Tomohiko、Nozu Kandai、Matsuo Masafumi、Zhao Jinghong
- Journal Title
  
  BMC Nephrology
  
  Volume: 22 Issue: 1
- DOI
  10.1186/s12882-021-02585-7
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K08726
[Journal Article] Systematic Review of Genotype-Phenotype Correlations in Frasier Syndrome2021
- Author(s)
  Tsuji Y, Yamamura T, Nagano C, Horinouchi T, Sakakibara N, Ishiko S, Aoto Y, Rossanti R, Okada E, Tanaka E, Tsugawa K, Okamoto T, Sawai T, Araki Y, Shima Y, Nakanishi K, Nagase H, Matsuo M, Iijima K, Nozu K.
- Journal Title
  
  Kidney Int Rep .
  
  Volume: 6 Issue: 10 Pages: 2585-2593
- DOI
  10.1016/j.ekir.2021.07.010
- NAID
  120007165718
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07799, KAKENHI-PROJECT-19K08726
[Journal Article] FAT1 biallelic truncating mutation causes a non-syndromic proteinuria in a child.2021
- Author(s)
  Rossanti R, Watanabe T, Nagano C, Hara S, Horinouchi T, Yamamura T, Sakakibara N, Ninchoji T, Iijima K, Nozu K.
- Journal Title
  
  CEN Case Reports
  
  Volume: 10(1) Issue: 1 Pages: 100-105
- DOI
  10.1007/s13730-020-00529-y
- Open Access
- Data Source
  KAKENHI-PROJECT-18KK0244
[Journal Article] Last Nucleotide Substitutions of COL4A5 Exons Cause Aberrant Splicing2021
- Author(s)
  Aoto Y, Horinouchi T, Yamamura T, Kondo A, Nagai S, Ishiko S, Okada E, Rossanti R, Sakakibara N, Nagano C, Awano H, Nagase H, Shima Y, Nakanishi K, Matsuo M, Iijima K, Nozu K.
- Journal Title
  
  Kidney Int Rep.
  
  Volume: 7 Issue: 1 Pages: 108-116
- DOI
  10.1016/j.ekir.2021.10.012
- NAID
  120007188929
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07799, KAKENHI-PROJECT-19K08726
[Journal Article] Functional analysis of suspected splicing variants in CLCN5 gene in Dent disease 1.2020
- Author(s)
  Inoue T, Nagano C, Matsuo M, Yamamura T, Sakakibara N, Horinouchi T, Shibagaki Y, Ichikawa D, Aoto Y, Ishiko S, Ishimori S, Rossanti R, Iijima K, Nozu K.
- Journal Title
  
  Clin Exp Nephrol
  
  Volume: in press Issue: 7 Pages: 606-612
- DOI
  10.1007/s10157-020-01876-x
- NAID
  120007028963
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-19K08726
[Journal Article] Pathogenic evaluation of synonymous COL4A5 variants in X‐linked Alport syndrome using a minigene assay2020
- Author(s)
  Horinouchi Tomoko、Yamamura Tomohiko、Minamikawa Shogo、Nagano China、Sakakibara Nana、Nakanishi Koichi、Shima Yuko、Morisada Naoya、Ishiko Shinya、Aoto Yuya、Nagase Hiroaki、Takeda Hiroki、Rossanti Rini、Ishimori Shingo、Kaito Hiroshi、Matsuo Masafumi、Iijima Kazumoto、Nozu Kandai
- Journal Title
  
  Molecular Genetics & Genomic Medicine
  
  Volume: 8 Issue: 8
- DOI
  10.1002/mgg3.1342
- NAID
  120006879547
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07799, KAKENHI-PROJECT-19K08726, KAKENHI-PROJECT-18K08243
[Journal Article] A Novel Truncating PAX2 Mutation in a Boy With Renal Coloboma Syndrome With Focal Segmental Glomerulosclerosis Causing Rapid Progression to End-Stage Kidney Disease2020
- Author(s)
  Saida K, Kamei K, Morisada N, Ogura M, Ogata K, Matsuoka K, Nozu K, Iijima K, Ito S.
- Journal Title
  
  CEN Case Rep
  
  Volume: 9 Issue: 1 Pages: 19-23
- DOI
  10.1007/s13730-019-00419-y
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18K08243, KAKENHI-PROJECT-18KK0244
[Journal Article] Comparison of clinical and genetic characteristics between Dent disease 1 and Dent disease 22020
- Author(s)
  Sakakibara Nana、Nagano China、Ishiko Shinya、Horinouchi Tomoko、Yamamura Tomohiko、Minamikawa Shogo、Shima Yuko、Nakanishi Koichi、Ishimori Shingo、Morisada Naoya、Iijima Kazumoto、Nozu Kandai
- Journal Title
  
  Pediatric Nephrology
  
  Volume: 35 Issue: 12 Pages: 2319-2326
- DOI
  10.1007/s00467-020-04701-5
- NAID
  120007052636
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18K07799, KAKENHI-PROJECT-19K08726, KAKENHI-PROJECT-18K08243
[Journal Article] Onset mechanism of a female patient with Dent disease 22020
- Author(s)
  Okamoto Takayuki、Sakakibara Nana、Nozu Kandai、Takahashi Toshiyuki、Hayashi Asako、Sato Yasuyuki、Nagano China、Matsuo Masafumi、Iijima Kazumoto、Manabe Atsushi
- Journal Title
  
  Clinical and Experimental Nephrology
  
  Volume: 24 Issue: 10 Pages: 946-954
- DOI
  10.1007/s10157-020-01926-4
- NAID
  120007160299
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K08726
[Journal Article] Genotype-phenotype correlations influence the response to angiotensin-targeting drugs in Japanese patients with male X-linked Alport syndrome2020
- Author(s)
  Yamamura Tomohiko、Horinouchi Tomoko、Nagano China、Omori Takashi、Sakakibara Nana、Aoto Yuya、Ishiko Shinya、Nakanishi Koichi、Shima Yuko、Nagase Hiroaki、Takeda Hiroki、Rossanti Rini、Ye Ming Juan、Nozu Yoshimi、Ishimori Shingo、Ninchoji Takeshi、Kaito Hiroshi、Morisada Naoya、Iijima Kazumoto、Nozu Kandai
- Journal Title
  
  Kidney International
  
  Volume: 98 Issue: 6 Pages: 1605-1614
- DOI
  10.1016/j.kint.2020.06.038
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07799, KAKENHI-PROJECT-19K08726, KAKENHI-PROJECT-18K08243
[Journal Article] Trimerization and genotype-phenotype correlation of COL4A5 mutants in Alport syndrome2020
- Author(s)
  Kamura Misato、Yamamura Tomohiko、Omachi Kohei、Suico Mary Ann、Nozu Kandai、Kaseda Shota、Kuwazuru Jun、Shuto Tsuyoshi、Iijima Kazumoto、Kai Hirofumi
- Journal Title
  
  Kidney International Reports
  
  Volume: - Issue: 5 Pages: 718-726
- DOI
  10.1016/j.ekir.2020.01.008
- NAID
  120006818746
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17H03570, KAKENHI-PROJECT-19H03379, KAKENHI-PROJECT-19J15443, KAKENHI-PROJECT-17K08309, KAKENHI-PROJECT-19K08726
[Journal Article] Development of an Exon Skipping Therapy for X-linked Alport Syndrome With Truncating Variants in COL4A5.2020
- Author(s)
  Yamamura T, Horinouchi T, Adachi T, Terakawa M, Takaoka Y, Omachi K, Takasato M, Takaishi K, Shoji T, Onishi Y, Kanazawa Y, Koizumi M, Tomono Y, Sugano S, Shono A, Minamikawa S, Nagano C, Sakakibara N, Ishiko S, Aoto Y, Kamura M, Harita Y, Miura K, Kanda S, Morisada N, and 6 others.
- Journal Title
  
  Nat Commun .
  
  Volume: 11(1) Issue: 1 Pages: 2777-2777
- DOI
  10.1038/s41467-020-16605-x
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K09921, KAKENHI-PROJECT-18K07887, KAKENHI-PROJECT-19K08726, KAKENHI-PROJECT-19K12202, KAKENHI-PROJECT-20K08584, KAKENHI-PROJECT-19H03379, KAKENHI-PROJECT-18K07414, KAKENHI-PROJECT-18K08243
[Journal Article] Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome2020
- Author(s)
  Jia Xiaoyuan、Yamamura Tomohiko、et al.
- Journal Title
  
  Kidney International
  
  Volume: 98 Issue: 5 Pages: 1308-1322
- DOI
  10.1016/j.kint.2020.05.029
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07799, KAKENHI-PROJECT-19K08726, KAKENHI-PROJECT-20K08370, KAKENHI-PROJECT-20K16892, KAKENHI-PROJECT-18KK0244, KAKENHI-PROJECT-20H03698
[Journal Article] Genetic background, recent advances in molecular biology, and development of novel therapy in Alport syndrome2020
- Author(s)
  Nozu Kandai、Takaoka Yutaka、Kai Hirofumi、Takasato Minoru、Yabuuchi Kensuke、Yamamura Tomohiko、Horinouchi Tomoko、Sakakibara Nana、Ninchoji Takeshi、Nagano China、Iijima Kazumoto
- Journal Title
  
  Kidney Research and Clinical Practice
  
  Volume: 39 Issue: 4 Pages: 402-413
- DOI
  10.23876/j.krcp.20.111
- NAID
  120006956375
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07887, KAKENHI-PROJECT-19K08726, KAKENHI-PROJECT-19H03379
[Journal Article] Molecular mechanisms determining severity in patients with Pierson syndrome2020
- Author(s)
  Minamikawa Shogo、Miwa Saori、Inagaki Tetsuji、Nishiyama Kei、Kaito Hiroshi、Ninchoji Takeshi、Yamamura Tomohiko、Nagano China、Sakakibara Nana、Ishimori Shingo、Hara Shigeo、Yoshikawa Norishige、Hirano Daishi、Harada Ryoko、Hamada Riku、Matsunoshita Natsuki、Nagata Michio、Shima Yuko、Nozu Kandai
- Journal Title
  
  Journal of Human Genetics
  
  Volume: 65 Issue: 4 Pages: 355-362
- DOI
  10.1038/s10038-019-0715-0
- NAID
  120006811107
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19K08726, KAKENHI-PROJECT-17K16087, KAKENHI-PROJECT-18K07799, KAKENHI-PROJECT-18K08243, KAKENHI-PROJECT-19K17297, KAKENHI-PROJECT-18KK0244
[Journal Article] Comprehensive genetic diagnosis of Japanese patients with severe proteinuria.2020
- Author(s)
  Nagano C, Yamamura T, Horinouchi T, Aoto Y, Ishiko S, Sakakibara N, Shima Y, Nakanishi K, Nagase H, Iijima K, Nozu K.
- Journal Title
  
  Sci Rep.
  
  Volume: 10(1) Issue: 1 Pages: 428-437
- DOI
  10.1038/s41598-019-57149-5
- NAID
  120006884200
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07799, KAKENHI-PROJECT-19K08726, KAKENHI-PROJECT-18KK0244, KAKENHI-PROJECT-18K15713
[Journal Article] Establishment of X-linked Alport syndrome model mice with a Col4a5 R471X mutation2019
- Author(s)
  Hashikami Kentarou、Asahina Makoto、Nozu Kandai、Iijima Kazumoto、Nagata Michio、Takeyama Michiyasu
- Journal Title
  
  Biochemistry and Biophysics Reports
  
  Volume: 17 Pages: 81-86
- DOI
  10.1016/j.bbrep.2018.12.003
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17H04189
[Journal Article] アルポート症候群2019
- Author(s)
  野津寛大、飯島一誠
- Journal Title
  
  指定難病ペディア,日本医師会雑誌
  
  Volume: 148 Pages: 249-249
- Data Source
  KAKENHI-PROJECT-17H04189
[Journal Article] Determination of the pathogenicity of known COL4A5 intronic variants by in vitro splicing assay.2019
- Author(s)
  Horinouchi T, Nozu K, Yamamura T, Minamikawa S, Nagano C, Sakakibara N, Nakanishi K, Shima Y, Morisada N, Ishiko S, Aoto Y, Nagase H, Takeda H, Rossanti R, Kaito H, Matsuo M, Iijima K.
- Journal Title
  
  Sci Rep.
  
  Volume: 9(1) Issue: 1 Pages: 12696-12696
- DOI
  10.1038/s41598-019-48990-9
- NAID
  120006825910
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07799, KAKENHI-PROJECT-18K08243, KAKENHI-PROJECT-19K08726, KAKENHI-PROJECT-17H04189, KAKENHI-PROJECT-18K15712
[Journal Article] Molecular assay for an intronic variant in NUP93 that causes steroid resistant nephrotic syndrome2019
- Author(s)
  Rossanti Rini、Shono Akemi、Miura Kenichiro、Hattori Motoshi、Yamamura Tomohiko、Nakanishi Keita、Minamikawa Shogo、Fujimura Junya、Horinouchi Tomoko、Nagano China、Sakakibara Nana、Kaito Hiroshi、Nagase Hiroaki、Morisada Naoya、Asanuma Katsuhiko、Matsuo Masafumi、Nozu Kandai、Iijima Kazumoto
- Journal Title
  
  Journal of Human Genetics
  
  Volume: 64 Issue: 7 Pages: 673-679
- DOI
  10.1038/s10038-019-0606-4
- NAID
  120006653286
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K08243, KAKENHI-PROJECT-19K09921, KAKENHI-PROJECT-18KK0244, KAKENHI-PROJECT-18K15712, KAKENHI-PROJECT-18H02823
[Journal Article] Comparison between conventional and comprehensive sequencing approaches for genetic diagnosis of Alport syndrome.2019
- Author(s)
  Yamamura T, Nozu K, Minamikawa S, Horinouchi T, Sakakibara N, Nagano C, Aoto Y, Ishiko S, Nakanishi K, Shima Y, Nagase H, Rossanti R, Ye MJ, Nozu Y, Ishimori S, Morisada N, Kaito H, Iijima K.
- Journal Title
  
  Mol Genet Genomic Med.
  
  Volume: 7(9) Issue: 9
- DOI
  10.1002/mgg3.883
- NAID
  120006733124
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07799, KAKENHI-PROJECT-18K08243, KAKENHI-PROJECT-19K08726, KAKENHI-PROJECT-17H04189
[Journal Article] Inherited salt‐losing tubulopathy: an old condition but a new category of tubulopathy2019
- Author(s)
  Nozu Kandai、Yamamura Tomohiko、Horinouchi Tomoko、Nagano China、Sakakibara Nana、Ishikura Kenji、Hamada Riku、Morisada Naoya、Iijima Kazumoto
- Journal Title
  
  Pediatrics International
  
  Volume: - Issue: 4 Pages: 428-437
- DOI
  10.1111/ped.14089
- NAID
  120006844963
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K08243, KAKENHI-PROJECT-19K08726
[Journal Article] Germline mosaicism is a pitfall in the diagnosis of “sporadic” X-linked Alport syndrome2018
- Author(s)
  Okamoto Takayuki、Nozu Kandai、Iijima Kazumoto、Ariga Tadashi
- Journal Title
  
  Journal of Nephrology
  
  Volume: 32 Issue: 1 Pages: 155-159
- DOI
  10.1007/s40620-018-0518-y
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17H04189
[Journal Article] Study protocol: mycophenolate mofetil as maintenance therapy after rituximab treatment for childhood-onset, complicated, frequently-relapsing nephrotic syndrome or steroid-dependent nephrotic syndrome: a multicenter double-blind, randomized, placebo-controlled trial (JSKDC07)2018
- Author(s)
  Horinouchi Tomoko、Sako Mayumi、Nakanishi Koichi、Ishikura Kenji、Ito Shuichi、Nakamura Hidefumi、Oba Mari Saito、Nozu Kandai、Iijima Kazumoto
- Journal Title
  
  BMC Nephrology
  
  Volume: 19 Issue: 1 Pages: 302-302
- DOI
  10.1186/s12882-018-1099-7
- NAID
  120006539303
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18KK0244
[Journal Article] Study protocol: high-dose mizoribine with prednisolone therapy in short-term relapsing steroid-sensitive nephrotic syndrome to prevent frequent relapse (JSKDC05 trial).2018
- Author(s)
  Hama T, Nakanishi K, Ishikura K, Ito S, Nakamura H, Sako M, Saito-Oba M, Nozu K, Shima Y, Iijima K, Yoshikawa N; Japanese Study Group of Kidney Disease in Children (JSKDC).
- Journal Title
  
  BMC Nephrol.
  
  Volume: 19 Issue: 1 Pages: 223-223
- DOI
  10.1186/s12882-018-1033-z
- NAID
  120006523804
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07799, KAKENHI-PROJECT-18KK0244, KAKENHI-PROJECT-15K09694
[Journal Article] Long-term clinicopathologic observation in a case of steroid-resistant nephrotic syndrome caused by a novel Crumbs homolog 2 mutation.2018
- Author(s)
  Watanabe S, Aizawa T, Tsukaguchi H, Tsugawa K, Tsuruga K, Shono A, Nozu K, Iijima K, Joh K, Tanaka H.
- Journal Title
  
  Nephrology (Carlton)
  
  Volume: - Issue: 7 Pages: 697-702
- DOI
  10.1111/nep.13244
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-16K10055, KAKENHI-PROJECT-16K10066, KAKENHI-PROJECT-17K09719, KAKENHI-PROJECT-18KK0244
[Journal Article] A review of clinical characteristics and genetic backgrounds in Alport syndrome2018
- Author(s)
  Nozu K, Nakanishi K, Abe Y, Udagawa T, Okada S, Okamoto T, Kaito H, Kanemoto K, Kobayashi A, Tanaka E, Tanaka K, Hama T, Fujimaru R, Miwa S, Yamamura T, Yamamura N, Horinouchi T, Minamikawa S, Nagata M, Iijima K
- Journal Title
  
  Clinical and Experimental Nephrology
  
  Volume: 23 Issue: 2 Pages: 158-168
- DOI
  10.1007/s10157-018-1629-4
- NAID
  120006557458
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-17H04189, KAKENHI-PROJECT-17H06658
[Journal Article] Rituximab in steroid-sensitive nephrotic syndrome: lessons from clinical trials2018
- Author(s)
  Iijima Kazumoto、Sako Mayumi、Kamei Koichi、Nozu Kandai
- Journal Title
  
  Pediatric Nephrology
  
  Volume: 33 Issue: 9 Pages: 1449-1455
- DOI
  10.1007/s00467-017-3746-9
- NAID
  120006498201
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18KK0244
[Journal Article] Strong Association of the HLA-DR/DQ Locus with Childhood Steroid-Sensitive Nephrotic Syndrome in the Japanese Population.2018
- Author(s)
  Jia X, Horinouchi T, Hitomi Y, Shono A, Khor SS, Omae Y, Kojima K, Kawai Y, Nagasaki M, Kaku Y, Okamoto T, Ohwada Y, Ohta K, Okuda Y, Fujimaru R, Hatae K, Kumagai N, Sawanobori E, Nakazato H, Ohtsuka Y, Nakanishi K, Shima Y, Tanaka R, Ashida A, Kamei K, Ishikura K, Nozu K, Tokunaga K, Iijima K
- Journal Title
  
  J Am Soc Nephrol.
  
  Volume: 29 Issue: 8 Pages: 2189-2199
- DOI
  10.1681/asn.2017080859
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18K07799, KAKENHI-PROJECT-18KK0244, KAKENHI-PLANNED-18H05511, KAKENHI-PROJECT-15K09694, KAKENHI-PROJECT-16K10066
[Journal Article] Ocular findings in a case of Pierson syndrome with a novel mutation in laminin ?2 gene2018
- Author(s)
  Arima Mitsuru、Tsukamoto Shoko、Akiyama Rumi、Nishiyama Kei、Kohno Ri-ichiro、Tachibana Takashi、Hayashida Akira、Murayama Miwa、Hisatomi Toshio、Nozu Kandai、Iijima Kazumoto、Ohga Shouichi、Sonoda Koh-Hei
- Journal Title
  
  Journal of American Association for Pediatric Ophthalmology and Strabismus
  
  Volume: 22 Issue: 5 Pages: 401-403.e1
- DOI
  10.1016/j.jaapos.2018.03.016
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18KK0244
[Journal Article] Detection of Splicing Abnormalities and Genotype-Phenotype Correlation in X-linked Alport Syndrome.2018
- Author(s)
  Horinouchi T, Nozu K, Yamamura T, Minamikawa S, Omori T, Nakanishi K, Fujimura J, Ashida A, Kitamura M, Kawano M, Shimabukuro W, Kitabayashi C, Imafuku A, Tamagaki K, Kamei K, Okamoto K, Fujinaga S, Oka M, Igarashi T, Miyazono A, Sawanobori E, Fujimaru R, Nakanishi K, Shima Y et al
- Journal Title
  
  J Am Soc Nephrol.
  
  Volume: 29 Issue: 8 Pages: 2244-2254
- DOI
  10.1681/asn.2018030228
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07799, KAKENHI-PROJECT-18K08243, KAKENHI-PROJECT-17H04189, KAKENHI-PROJECT-15K09694
[Journal Article] 【腎臓学　この一年の進歩】遺伝性腎疾患2018
- Author(s)
  野津寛大, 飯島一誠
- Journal Title
  
  日本腎臓学会誌
  
  Volume: 61巻1号 Pages: 18-22
- Data Source
  KAKENHI-PROJECT-17H04189
[Journal Article] Development of ultra-deep targeted RNA sequencing for analyzing X-chromosome inactivation in female Dent disease2018
- Author(s)
  Minamikawa S, Nozu K, Nozu Y, Yamamura T, Taniguchi-Ikeda M, Nakanishi K, Fujimura J, Horinouchi T, Shima Y, Nakanishi K, Hattori M, Kanda K, Tanaka R, Morisada N, Nagano C, Sakakibara N, Nagase H, Morioka I, Kaito H, Iijima K.
- Journal Title
  
  Journal of Human Genetics
  
  Volume: 63 Issue: 5 Pages: 589-595
- DOI
  10.1038/s10038-018-0415-1
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15K09694, KAKENHI-PROJECT-15K09261, KAKENHI-PROJECT-15K09691, KAKENHI-PROJECT-18K07799, KAKENHI-PROJECT-18K08243
[Journal Article] Pair analysis and custom array CGH can detect a small copy number variation in COQ6 gene2018
- Author(s)
  Nakanishi Keita、Okamoto Takayuki、Nozu Kandai、Hara Shigeo、Sato Yasuyuki、Hayashi Asako、Takahashi Toshiyuki、Nagano China、Sakakibara Nana、Horinouchi Tomoko、Fujimura Junya、Minamikawa Shogo、Yamamura Tomohiko、Rossanti Rini、Nagase Hiroaki、Kaito Hiroshi、Ariga Tadashi、Iijima Kazumoto
- Journal Title
  
  Clinical and Experimental Nephrology
  
  Volume: 23 Issue: 5 Pages: 669-675
- DOI
  10.1007/s10157-018-1682-z
- NAID
  120006644119
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18KK0244, KAKENHI-PROJECT-17K16262, KAKENHI-PROJECT-18K15712
[Journal Article] Detection of copy number variations by pair analysis using next-generation sequencing data in inherited kidney diseases2018
- Author(s)
  Nagano C, Nozu K, Morisada N, Yazawa M, Ichikawa D, Numasawa K, Kourakata H, Matsumura C, Tazoe S, Tanaka R, Yamamura T, Minamikawa S, Horinouchi T, Nakanishi K, Fujimura J, Sakakibara N, Nozu Y, Ye MJ, Kaito H, Iijima K
- Journal Title
  
  Clinical and Experimental Nephrology
  
  Volume: 印刷中 Issue: 4 Pages: 881-888
- DOI
  10.1007/s10157-018-1534-x
- NAID
  120006624236
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-17H04189, KAKENHI-PROJECT-15K09261, KAKENHI-PROJECT-15K09691, KAKENHI-PROJECT-16K19642, KAKENHI-PROJECT-18K08243
[Journal Article] The utility of urinary CD80 as a diagnostic marker in patients with renal diseases2018
- Author(s)
  Minamikawa Shogo、Nozu Kandai、Maeta Shingo、Yamamura Tomohiko、Nakanishi Keita、Fujimura Junya、Horinouchi Tomoko、Nagano China、Sakakibara Nana、Nagase Hiroaki、Shima Hideaki、Noda Kenta、Ninchoji Takeshi、Kaito Hiroshi、Iijima Kazumoto
- Journal Title
  
  Scientific Reports
  
  Volume: 8 Issue: 1 Pages: 17322-17322
- DOI
  10.1038/s41598-018-35798-2
- NAID
  120006543320
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18KK0244
[Journal Article] Clinical and Genetic Characteristics in Patients With Gitelman Syndrome.2018
- Author(s)
  Fujimura J, Nozu K, Yamamura T, Minamikawa S, Nakanishi K, Horinouchi T, Nagano C, Sakakibara N, Nakanishi K, Shima Y, Miyako K, Nozu Y, Morisada N, Nagase H, Ninchoji T, Kaito H, Iijima K.
- Journal Title
  
  Kidney Int Rep.
  
  Volume: ４ Issue: 1 Pages: 119-125
- DOI
  10.1016/j.ekir.2018.09.015
- NAID
  120006847258
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-18K07799, KAKENHI-PROJECT-18K08243, KAKENHI-PROJECT-15K09694, KAKENHI-PROJECT-19K08726
[Journal Article] Rituximab therapy for refractory steroid-resistant nephrotic syndrome in children2018
- Author(s)
  Kamei Koichi、Ishikura Kenji、Sako Mayumi、Ito Shuichi、Nozu Kandai、Iijima Kazumoto
- Journal Title
  
  Pediatric Nephrology
  
  Volume: 印刷中 Issue: 1 Pages: 17-24
- DOI
  10.1007/s00467-018-4166-1
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-18KK0244
[Journal Article] ステロイド感受性ネフローゼ症候群とゲノムワイド関連解析2018
- Author(s)
  飯島一誠, 堀之内智子, 野津寛大
- Journal Title
  
  【ネフローゼ症候群-MCNS/FSGSの最新知見】病因、病態、病理学
  
  Volume: 85巻6号 Pages: 777-781
- Data Source
  KAKENHI-PROJECT-18KK0244
[Journal Article] Functional splicing analysis in an infantile case of atypical hemolytic uremic syndrome caused by digenic mutations in C3 and MCP genes2018
- Author(s)
  Yamamura Tomohiko、Nozu Kandai、Ueda Hiroaki、Fujimaru Rika、Hisatomi Ryutaro、Yoshida Yoko、Kato Hideki、Nangaku Masaomi、Miyata Toshiyuki、Sawai Toshihiro、Minamikawa Shogo、Kaito Hiroshi、Matsuo Masafumi、Iijima Kazumoto
- Journal Title
  
  Journal of Human Genetics
  
  Volume: Epub ahead of print Issue: 6 Pages: 755-759
- DOI
  10.1038/s10038-018-0436-9
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-17K16073, KAKENHI-PROJECT-15K09691, KAKENHI-PROJECT-16K09834
[Journal Article] Cryptic exon activation in SLC12A3 in Gitelman syndrome.2017
- Author(s)
  Nozu K, Nozu Y, Nakanishi K, Konomoto T, Horinouchi T, Shono A, Morisada N, Minamikawa S, Yamamura T, Fujimura J, Nakanishi K, Ninchoji T, Kaito H, Morioka I, Taniguchi-Ikeda M, Vorechovsky I, Iijima K
- Journal Title
  
  J Hum Genet.
  
  Volume: 62 Issue: 2 Pages: 335-337
- DOI
  10.1038/jhg.2016.129
- NAID
  40021065185
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-26461632, KAKENHI-PROJECT-15K09261, KAKENHI-PROJECT-15K09691, KAKENHI-PROJECT-16K10066
[Journal Article] A comparison of splicing assays to detect an intronic variant of the OCRL gene in Lowe syndrome2017
- Author(s)
  Nakanishi Keita、Nozu Kandai、Hiramoto Ryugo、Minamikawa Shogo、Yamamura Tomohiko、Fujimura Junya、Horinouchi Tomoko、Ninchoji Takeshi、Kaito Hiroshi、Morisada Naoya、Ishimori Shingo、Nakanishi Koichi、Morioka Ichiro、Awano Hiroyuki、Matsuo Masafumi、Iijima Kazumoto
- Journal Title
  
  European Journal of Medical Genetics
  
  Volume: 60 Issue: 12 Pages: 631-634
- DOI
  10.1016/j.ejmg.2017.08.001
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15K09691
[Journal Article] A case of mild phenotype Alport syndrome caused by COL4A3 mutations2017
- Author(s)
  Kamijo Masafumi、Kitamura Mineaki、Muta Kumiko、Uramatsu Tadashi、Obata Yoko、Nozu Kandai、Kaito Hiroshi、Iijima Kazumoto、Mukae Hiroshi、Nishino Tomoya
- Journal Title
  
  CEN Case Reports
  
  Volume: 6 Issue: 2 Pages: 189-193
- DOI
  10.1007/s13730-017-0273-2
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-17H04189
[Journal Article] Natural history and genotype-phenotype correlation in female X-linked Alport syndrome.2017
- Author(s)
  Yamamura T, Nozu K, Fu XJ, Nozu Y, Ye MJ, Shono A, Yamanouchi S, Minamikawa S, Morisada N, Nakanishi K, Shima Y, Yoshikawa N, Ninchoji T, Morioka I, Kaito H, Iijima K
- Journal Title
  
  Kideny Int Rep.
  
  Volume: 印刷中
- NAID
  120006373817
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-26293203
[Journal Article] Natural History and Genotype?Phenotype Correlation in Female X-Linked Alport Syndrome2017
- Author(s)
  Yamamura Tomohiko、Nozu Kandai、Fu Xue Jun、Nozu Yoshimi、Ye Ming Juan、Shono Akemi、Yamanouchi Satoko、Minamikawa Shogo、Morisada Naoya、Nakanishi Koichi、Shima Yuko、Yoshikawa Norishige、Ninchoji Takeshi、Morioka Ichiro、Kaito Hiroshi、Iijima Kazumoto
- Journal Title
  
  Kidney Int Rep.
  
  Volume: 2 Issue: 5 Pages: 850-855
- DOI
  10.1016/j.ekir.2017.04.011
- NAID
  120006373817
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15K09694, KAKENHI-PROJECT-16K10066, KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-17H04189, KAKENHI-PROJECT-15K09695, KAKENHI-PROJECT-16K19642
[Journal Article] Detection of a Splice Site Variant in a Patient with Glomerulopathy and Fibronectin Deposits2017
- Author(s)
  Tsuji Yurika、Nozu Kandai、Sofue Tadashi、Hara Shigeo、Nakanishi Keita、Yamamura Tomohiko、Minamikawa Shogo、Nozu Yoshimi、Kaito Hiroshi、Fujimura Junya、Horinouchi Tomoko、Morisada Naoya、Morioka Ichiro、Taniguchi-Ikeda Mariko、Matsuo Masafumi、Iijima Kazumoto
- Journal Title
  
  Nephron
  
  Volume: 138 Issue: 2 Pages: 166-171
- DOI
  10.1159/000484209
- NAID
  120006867371
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15K09691
[Journal Article] Characterization of contiguous gene deletions in COL4A6 and COL4A5 in Alport syndrome-diffuse leiomyomatosis.2017
- Author(s)
  Nozu K, Minamikawa S, Yamada S, Oka M, Yanagita M, Morisada N, Fujinaga S, Nagano C, Gotoh Y, Takahashi E, Morishita T, Yamamura T, Ninchoji T, Kaito H, Morioka I, Nakanishi K, Vorechovsky I, Iijima K
- Journal Title
  
  J Hum Genet.
  
  Volume: Epub 2017 Mar 9. Issue: 7 Pages: 733-735
- DOI
  10.1038/jhg.2017.28
- Peer Reviewed / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-26461632, KAKENHI-PROJECT-17H04189
[Journal Article] Autosomal dominant form of type IV collagen nephropathy exists among patients with hereditary nephritis difficult to diagnose clinicopathologically2017
- Author(s)
  Imafuku Aya、Nozu Kandai、Sawa Naoki、Hasegawa Eiko、Hiramatsu Rikako、Kawada Masahiro、Hoshino Junichi、Tanaka Kiho、Ishii Yasuo、Takaichi Kenmei、Fujii Takeshi、Ohashi Kenichi、Iijima Kazumoto、Ubara Yoshifumi
- Journal Title
  
  Nephrology
  
  Volume: 印刷中 Issue: 10 Pages: 940-947
- DOI
  10.1111/nep.13115
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-17H04189
[Journal Article] Diagnostic strategy for inherited hypomagnesemia.2017
- Author(s)
  Horinouchi T, Nozu K, Kamiyoshi N, Kamei K, Togawa H, Shima Y, Urahama Y, Yamamura T, Minamikawa S, Nakanishi K, Fujimura J, Morioka I, Ninchoji T, Kaito H, Nakanishi K, Iijima K.
- Journal Title
  
  Clin Exp Nephrol.
  
  Volume: 印刷中 Issue: 6 Pages: 1003-1010
- DOI
  10.1007/s10157-017-1396-7
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15K09694, KAKENHI-PROJECT-15K09691
[Journal Article] An in vitro splicing assay reveals the pathogenicity of a novel intronic variant in ATP6V0A4 for autosomal recessive distal renal tubular acidosis2017
- Author(s)
  Yamamura Tomohiko、Nozu Kandai、Miyoshi Yuya、Nakanishi Keita、Fujimura Junya、Horinouchi Tomoko、Minamikawa Shogo、Mori Nobuo、Fujimaru Rika、Nakanishi Koichi、Ninchoji Takeshi、Kaito Hiroshi、Mariko Taniguchi-Ikeda、Morioka Ichiro、Matsuo Masafumi、Iijima Kazumoto
- Journal Title
  
  BMC Nephrology
  
  Volume: 18 Issue: 1 Pages: 353-353
- DOI
  10.1186/s12882-017-0774-4
- NAID
  120006377621
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15K09691
[Journal Article] A Novel Mutation in a Japanese Family with X-linked Alport Syndrome.2016
- Author(s)
  Abe Y, Iyoda M, Nozu K, Hibino S, Hihara K, Yamaguchi Y, Yamamura T, Minamikawa S, Iijima K, Shibata T, Itabashi K
- Journal Title
  
  Intern Med.
  
  Volume: 55 Pages: 2843-2847
- NAID
  130005605859
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26293203
[Journal Article] Early RAAS Blockade Exerts Renoprotective Effects in Autosomal Recessive Alport Syndrome.2016
- Author(s)
  Uchida N, Kumagai N, Nozu K, Fu XJ, Iijima K, Kondo Y, Kure S
- Journal Title
  
  Tohoku J Exp Med.
  
  Volume: 240 Pages: 251-257
- NAID
  130005170640
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26293203
[Journal Article] Pathogenesis of hypokalemia in autosomal dominant hypocalcemia type 1.2016
- Author(s)
  Kamiyoshi N, Nozu K, Urahama Y, Matsunoshita N, Yamamura T, Minamikawa S, Ninchoji T, Morisada N, Nakanishi K, Kaito H, Iijima K.
- Journal Title
  
  Clin Exp Nephrol.
  
  Volume: 20 Issue: 2 Pages: 253-257
- DOI
  10.1007/s10157-015-1160-9
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-15K09691, KAKENHI-PROJECT-26461618, KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-26860800, KAKENHI-PROJECT-15K09261
[Journal Article] Identification of mutations　in FN1 leading to glomerulopathy with fibronectin deposits.2016
- Author(s)
  Ohtsubo H, Okada T, Nozu K, Takaoka Y, Shono A, Asanuma K, Zhang L, Nakanishi K, Taniguchi-Ikeda M, Kaito H, Iijima K, Nakamura SI
- Journal Title
  
  Pediatr Nephrol.
  
  Volume: 58 Issue: 9 Pages: 1459-1467
- DOI
  10.1007/s00467-016-3368-7
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-16K10066
[Journal Article] Rare renal ciliopathies in non-consanguineous families that were identified by targeted resequencing.2016
- Author(s)
  Yamamura T, Morisada N, Nozu K, Minamikawa S, Ishimori S, Toyoshima D, Ninchoji T, Yasui M, Taniguchi-Ikeda M, Morioka I, Nakanishi K, Nishio H, Iijima K.
- Journal Title
  
  Clin Exp Nephrol.
  
  Volume: 20 Issue: 1 Pages: 136-142
- DOI
  10.1007/s10157-016-1256-x
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-26461632, KAKENHI-PROJECT-15K09261
[Journal Article] 腎・泌尿器 Bartter症候群2016
- Author(s)
  野津寛大
- Journal Title
  
  小児科診療
  
  Volume: 79 Pages: 294-294
- Data Source
  KAKENHI-PROJECT-15K09691
[Journal Article] 腎・泌尿器 Gitelman症候群2016
- Author(s)
  野津寛大
- Journal Title
  
  小児科診療
  
  Volume: 79 Pages: 300-300
- Data Source
  KAKENHI-PROJECT-15K09691
[Journal Article] Female X-linked Alport syndrome with somatic mosaicism2016
- Author(s)
  Yokota K, Nozu K, Minamikawa S, Yamamura T, Nakanishi K, Kaneda H, Hamada R, Nozu Y, Shono A, Ninchoji T, Morisada N, Ishimori S, Fujimura J, Horinouchi T, Kaito H, Nakanishi K, Morioka I, Taniguchi-Ikeda M, Iijima K.
- Journal Title
  
  Clin Exp Nephrol.
  
  Volume: 印刷中 Issue: 5 Pages: 877-883
- DOI
  10.1007/s10157-016-1352-y
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-15K09261, KAKENHI-PROJECT-16K10066, KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-17H04189, KAKENHI-PROJECT-16K19642
[Journal Article] Somatic mosaicism and variant frequency detected by next-generation sequencing in X-linked Alport syndrome.2016
- Author(s)
  Fu XJ, Nozu K, Kaito H, Ninchoji T, Morisada N, Nakanishi K, Yoshikawa N, Ohtsubo H, Matsunoshita N, Kamiyoshi N, Matsumura C, Takagi N, Maekawa K, Taniguchi-Ikeda M, Iijima K
- Journal Title
  
  Eur J Hum Genet
  
  Volume: 24 Issue: 3 Pages: 387-391
- DOI
  10.1038/ejhg.2015.113
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26461618, KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-26860800, KAKENHI-PROJECT-15K09695
[Journal Article] Next-generation sequencing discloses a nonsense mutation in the dystrophin gene from long preserved dried umbilical cord and low-level somatic mosaicism in the proband mother.2016
- Author(s)
  Taniguchi-Ikeda M, Takeshima Y, Lee T, Nishiyama M, Awano H, Yagi M, Unzaki A, Nozu K, Nishio H, Matsuo M, Kurahashi H, Toda T, Morioka I, Iijima K.
- Journal Title
  
  J Hum Genet.
  
  Volume: 61 Issue: 4 Pages: 351-355
- DOI
  10.1038/jhg.2015.157
- NAID
  40020802923
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-15K09621, KAKENHI-PROJECT-26253057, KAKENHI-PROJECT-15H04710, KAKENHI-PROJECT-26461632
[Journal Article] Differential diagnosis of Bartter syndrome, Gitelman syndrome, and pseudo-Bartter/Gitelman syndrome based on clinical characteristics2016
- Author(s)
  Matsunoshita N, Nozu K, Shono A, Nozu Y, Fu XJ, Morisada N, Kamiyoshi N, Ohtsubo H, Ninchoji T, Minamikawa S, Yamamura T, Nakanishi K, Yoshikawa N, Shima Y, Kaito H, Iijima K
- Journal Title
  
  Genetics in Medicine
  
  Volume: 18 Issue: 2 Pages: 180-188
- DOI
  10.1038/gim.2015.56
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-15K09691, KAKENHI-PROJECT-15K09694, KAKENHI-PROJECT-26461618, KAKENHI-PROJECT-26860800, KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-15K09695
[Journal Article] Genetic, clinical and pathological backgrounds in autosomal dominant Alport syndrome.2016
- Author(s)
  Kamiyoshi N, Nozu K, Fu XJ, Morisada N, Nozu Y, Imafuku A, Miura K, Yamamura T, Minamikawa S, Shono A, Ninchoji T, Kaito H, Morioka I, Nakanishi K, Yoshikawa N, Iijima K.
- Journal Title
  
  Clin J Am Soc Nephrol.
  
  Volume: 11
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26293203
[Journal Article] Female X-linked Alport syndrome with somatic mosaicism.2016
- Author(s)
  Yokota K, Nozu K, Minamikawa S, Yamamura T, Nakanishi K, Kaneda H, Hamada R, Nozu Y, Shono A, Ninchoji T, Morisada N, Ishimori S, Fujimura J, Horinouchi T, Kaito H, Nakanishi K, Morioka I, Taniguchi-Ikeda M, Iijima K
- Journal Title
  
  Clin Exp Nephrol.
  
  Volume: Epub 2016 Oct 31.
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26293203
[Journal Article] Genetic, Clinical, and Pathologic Backgrounds of Patients with Autosomal Dominant Alport Syndrome.2016
- Author(s)
  Kamiyoshi N, Nozu K, Fu XJ, Morisada N, Nozu Y, Ye MJ, Imafuku A, Miura K, Yamamura T, Minamikawa S, Shono A, Ninchoji T, Morioka I, Nakanishi K, Yoshikawa N, Kaito H, Iijima K
- Journal Title
  
  Clin J Am Soc Nephrol.
  
  Volume: 11 Issue: 8 Pages: 1441-1449
- DOI
  10.2215/cjn.01000116
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-15K09261, KAKENHI-PROJECT-15K09682, KAKENHI-PROJECT-15K09695, KAKENHI-PROJECT-16K10066
[Journal Article] Acute kidney injury in type 3 Bartter syndrome: Angiotensin-converting enzyme inhibitors as a cause.2016
- Author(s)
  Nagao R, Suzuki S, Kawashima H, Nozu K, Iijima K
- Journal Title
  
  Pediatr Int
  
  Volume: 58 Issue: 12 Pages: 1373-1374
- DOI
  10.1111/ped.13100
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15K09691
[Journal Article] Combined Alport syndrome and Klinefelter syndrome.2016
- Author(s)
  Nishida M, Hashimoto F, Kaito H, Nozu K, Iijima K, Asada D, Hamaoka K.
- Journal Title
  
  Pediatr Int.
  
  Volume: 58 Issue: 2 Pages: 152-155
- DOI
  10.1111/ped.12743
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26293203
[Journal Article] Biallelic mutations in nuclear pore complex subunit NUP107 cause early-childhood-onset steroid-resistant nephrotic syndrome2015
- Author(s)
  Miyake N, Tsukaguchi H, Koshimizu E, Shono A, Matsunaga S, Shiina M, Mimura Y, Imamura S, Hirose T, Okudela K, Nozu K, Akioka Y, Hattori M, Yoshikawa N, Kitamura A, Cheong HI, Kagami S, Yamashita M, Fujita A, Miyatake S, Tsurusaki Y, Nakashima M, Saitsu H, Ohashi K, Imamoto N, Ryo A, Ogata K, Iijima K, Matsumoto N
- Journal Title
  
  Am J Hum Genet
  
  Volume: 97(4) Issue: 4 Pages: 555-566
- DOI
  10.1016/j.ajhg.2015.08.013
- Peer Reviewed / Open Access / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26330331, KAKENHI-PROJECT-26461246, KAKENHI-PROJECT-26461549, KAKENHI-PROJECT-15K19660, KAKENHI-ORGANIZER-24118001, KAKENHI-PLANNED-24118005, KAKENHI-PLANNED-24118007, KAKENHI-PROJECT-25293235, KAKENHI-PROJECT-26293203
[Journal Article] Rituximab Treatment for Nephrotic Syndrome in Children.2015
- Author(s)
  Iijima K, Sako M, Nozu K.
- Journal Title
  
  Curr Pediatr Rep.
  
  Volume: 3 Issue: 1 Pages: 71-77
- DOI
  10.1007/s40124-014-0065-5
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26293203
[Journal Article] Alport症候群の軽症亜型2015
- Author(s)
  野津寛大、飯島一誠
- Journal Title
  
  Annual Review2015腎臓
  
  Volume: 2015 Pages: 75-79
- Data Source
  KAKENHI-PROJECT-25893131
[Journal Article] Long-term outcome of childhood IgA nephropathy with minimal proteinuria.2015
- Author(s)
  Higa A, Shima Y, Hama T, Sato M, Mukaiyama H, Togawa H, Tanaka R, Nozu K, Sako M, Iijima K, Nakanishi K, Yoshikawa N.
- Journal Title
  
  Pediatr Nephrol.
  
  Volume: 30(12) Issue: 12 Pages: 2121-7
- DOI
  10.1007/s00467-015-3176-5
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15K09694, KAKENHI-PROJECT-15K09695, KAKENHI-PROJECT-26461618, KAKENHI-PROJECT-26293203
[Journal Article] X-linked Alport syndrome associated with a synonymous p.Gly292Gly mutation alters the splicing donor site of the type IV collagen alpha chain 5 gene.2015
- Author(s)
  Fu XJ, Nozu K, Eguchi A, Nozu Y, Morisada N, Shono A, Taniguchi-Ikeda M, Shima Y, Nakanishi K, Vorechovsky I, Iijima K
- Journal Title
  
  Clin Exp Nephrol.
  
  Volume: 20 Issue: 5 Pages: 699-702
- DOI
  10.1007/s10157-015-1197-9
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-15K09261
[Journal Article] Bartter症候群、Gitelman症候群2015
- Author(s)
  松野下夏樹　野津寛大　飯島一誠
- Journal Title
  
  日本腎臓学会誌
  
  Volume: 57 Pages: 743-750
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-15K09691
[Journal Article] Bartter症候群・Gitelman症候群:遺伝性塩類喪失性尿細管機能異常症2015
- Author(s)
  野津寛大
- Journal Title
  
  内科
  
  Volume: ６ Pages: 1039-1039
- Data Source
  KAKENHI-PROJECT-15K09691
[Journal Article] Natural history of genetically proven autosomal recessive Alport syndrome2014
- Author(s)
  Oka M, Nozu K, Kaito H, Fu XJ, Nakanishi K, Hashimura Y, Morisada N, Yan K, Matsuo M, Yoshikawa N, Vorechovsky I, Iijima K
- Journal Title
  
  Pediatr Nephrol
  
  Volume: 29 Issue: 9 Pages: 1535-1544
- DOI
  10.1007/s00467-014-2797-4
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24390265, KAKENHI-PROJECT-25893131, KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-26461618
[Journal Article] X-Linked Alport Syndrome Caused by Splicing Mutations in COL4A52014
- Author(s)
  Nozu, K. Vorechovsky, I. Kaito, H. Fu, X. J. Nakanishi, K. Hashimura, Y. Hashimoto, F. Kamei, K. Ito, S. Kaku, Y. Imasawa, T. Ushijima, K. Shimizu, J. Makita, Y. Konomoto, T. Yoshikawa, N. Iijima, K.
- Journal Title
  
  Clinical journal of the American Society of Nephrology : CJASN
  
  Volume: 9 Issue: 11 Pages: 1958-64
- DOI
  10.2215/cjn.04140414
- Peer Reviewed / Acknowledgement Compliant
- Data Source
  KAKENHI-PROJECT-25893131, KAKENHI-PROJECT-26293203
[Journal Article] 【内科疾患最新の治療-明日への指針】Alport症候群2014
- Author(s)
  野津寛大、飯島一誠
- Journal Title
  
  内科
  
  Volume: 6 Pages: 1172-1173
- Data Source
  KAKENHI-PROJECT-26293203
[Journal Article] Milder clinical aspects of X-linked Alport syndrome in men positive for the collagen IV α5 chain2014
- Author(s)
  Hashimura Y, Nozu K, Kaito H, Nakanishi K, Fu XJ, Ohtsubo H, Hashimoto F, Oka M, Ninchoji T, Ishimori S, Morisada N, Matsunoshita N, Kamiyoshi N, Yoshikawa N, Iijima K
- Journal Title
  
  Kidney Int
  
  Volume: 85 Issue: 5 Pages: 1208-1213
- DOI
  10.1038/ki.2013.479
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-24390265, KAKENHI-PROJECT-25893131, KAKENHI-PROJECT-26293203, KAKENHI-PROJECT-26461618
[Journal Article] Alport syndrome caused by a COL4A5 deletion and exonization of an adjacent AluY.2014
- Author(s)
  Nozu K, Iijima K, Ohtsuka Y, Fu XJ, Kaito H, Nakanishi K, Vorechovsky I
- Journal Title
  
  Mol Genet Genomic Med
  
  Volume: 2 Issue: 5 Pages: 451-451
- DOI
  10.1002/mgg3.89
- Peer Reviewed / Open Access
- Data Source
  KAKENHI-PROJECT-25461648, KAKENHI-PROJECT-25893131, KAKENHI-PROJECT-26293203
[Journal Article] Alport症候群2014
- Author(s)
  野津寛大、飯島一誠
- Journal Title
  
  内科
  
  Volume: 6 Pages: 1172-73
- NAID
  10025170337
- Data Source
  KAKENHI-PROJECT-25893131
[Journal Article] Recurrent Deep Intronic Mutations in the SLC12A3 Gene Responsible for Gitelman's Syndrome.2011
- Author(s)
  Lo YF, Nozu K, Iijima K, Morishita T, Huang CC, Yang SS, Sytwu HK, Fang YW, Tseng MH, Lin SH.
- Journal Title
  
  Clin J Am Soc Nephrol. 6(3)
  
  Pages: 630-639
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] Epithelial-to-mesenchymal transition in cyst lining epithelial cells in an orthologous PCK rat model of autosomal-recessive polycystic kidney disease2011
- Author(s)
  Togawa H, Nakanishi K, Mukaiyama H, Hama T, Shima Y, Sako M, Miyajima M, Nozu K, Nishii K, Nagao S, Takahashi H, Iijima K, Yoshikawa N
- Journal Title
  
  Am J Physiol Renal Physiol
  
  Volume: 300
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] Branchio-oto-renal syndrome caused by partial EYA1 deletion due to LINE-1 insertion2010
- Author(s)
  Morisada N, Rendtorff ND, Nozu K, Morishita T, Miyakawa T, Matsumoto T, Hisano S, Iijima K, Tranebjaerg L, Shirahata A, Matsuo M, Kusuhara K.
- Journal Title
  
  Pediatr Nephrol
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article]2010
- Author(s)
  中山真紀子, 野津寛大, 飯島一誠
- Journal Title
  
  TCF2遺伝子異常と先天性腎尿路奇形『Annual Review 腎臓2010』(御手洗哲也・東原英二編)(中外医学社)
  
  Pages: 212-218
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] HNF1B Alterations Associated with Congenital Anomalies of the Kidney and Urinary Tract.2010
- Author(s)
  Nakayama M, Nozu K, Goto Y, Kamei K, Ito S, Sato H, Emi M, Nakanishi K, Tuchiya S, Iijima K.
- Journal Title
  
  Pediatr Nephrol 25(6)
  
  Pages: 1073-1079
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] The Pharmacological Characteristics of Molecular-Based Inherited Salt-Losing Tubulopathies.2010
- Author(s)
  Nozu K, Iijima K, Kanda K, Nakanishi K, Yoshikawa N, Satomura K, Kaito H, Hashimura Y, Ninchoji T, Komatsu H, Kamei K, Miyashita R, Kugo M, Ohashi H, Yamazaki H, Mabe H, Otsubo A, Igarashi T, Matsuo M.
- Journal Title
  
  J Clin Endocrinol Metab. 95(12)
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] Branchio-oto-renal syndrome caused by partial EYA1 deletion due to LINE-1 insertion2010
- Author(s)
  Morisada N, Rendtorff ND, Nozu K, Morishita T, Miyakawa T, Matsumoto T, Hisano S, Iijima K, Tranebjaerg L, Shirahata A, Matsuo M, Kusuhara K
- Journal Title
  
  Pediatr Nephrol
  
  Volume: 25 Pages: 1343-1348
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] A family with X-linked benign familial hematuria2010
- Author(s)
  Kaneko K, Tanaka S, Hasui M, Nozu K, Krol RP, Iijima K, Sugimoto K, Takemura T
- Journal Title
  
  Pediatr Nephrol
  
  Volume: 25 Pages: 545-548
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] 常染色体性Alport症候群2010
- Author(s)
  岡政史, 野津寛大, 飯島一誠, 松尾雅文
- Journal Title
  
  日本小児腎臓病学会雑誌
  
  Volume: 23 Pages: 8-12
- NAID
  10026412082
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] HNF1B alterations associated with congenital anomalies of the kidney and urinary tract2010
- Author(s)
  Nakayama M, Nozu K, Goto Y, Kamei K, Ito S, Sato H, Emi M, Nakanishi K, Tsuchiya S, Iijima K
- Journal Title
  
  Pediatr Nephrol
  
  Volume: 25 Pages: 1073-79
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] 運動後急性腎不全とPRES(Posterior reversible encephalopathy syndrome)の合併を反復した腎性低尿酸血症の1例2010
- Author(s)
  島友子, 中西浩一, 戸川寛子, 野津寛大, 飯島一誠, 吉川徳茂
- Journal Title
  
  日本小児腎不全学会雑誌
  
  Volume: 30 Pages: 145-146
- NAID
  10027697727
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article]2010
- Author(s)
  神田杏子, 野津寛大, 飯島一誠, 松尾雅文
- Journal Title
  
  Bartter 症候群と Gitelman 症候群についての最近の知見・利尿剤負荷試験にて判明したこと『Annual Review 腎臓2010』(御手洗哲也・東原英二編)(中外医学社)
  
  Pages: 72-77
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] 集学的治療により救命しえたPotter sequenceの1例2010
- Author(s)
  忍頂寺毅史, 藤岡一路, 橋村裕也, 貝藤裕史, 森岡一朗, 野津寛大, 横山直樹, 飯島一誠, 松尾雅文
- Journal Title
  
  日本小児腎不全学会雑誌
  
  Volume: 30 Pages: 178-180
- NAID
  10027697824
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] ヒト常染色体劣性多発性嚢胞腎(ARPKD)相同遺伝子ラットモデル(PCKラット)の尿細管上皮細胞における上皮間葉移行(EMT)2010
- Author(s)
  戸川寛子, 中西浩一, 島友子, 佐古まゆみ, 宮嶋正康, 野津寛大, 飯島一誠, 吉原大輔, 長尾枝澄香, 吉川徳茂
- Journal Title
  
  発達腎研究会誌
  
  Volume: 18 Pages: 10-13
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] COL4A3/COL4A4のヘテロ接合体変異を有する菲薄基底膜腎症のドナーから生体腎移植を実施した常染色体劣性アルポート症候群の2例2010
- Author(s)
  梶保祐子, 上田博章, 水谷誠, 谷口貴実子, 古山政幸, 石塚喜世伸, 藤井寛, 近本裕子, 秋岡祐子, 岡政史, 野津寛大, 飯島一誠, 服部元史
- Journal Title
  
  日本小児腎臓病学会雑誌
  
  Volume: 23 Pages: 113-118
- NAID
  130000814249
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] Branchio-oto-renal syndrome caused by partial EYA1 deletion due to LINE-1 insertion.2010
- Author(s)
  Morisada N, Rendtorff ND, Nozu K, Morishita T, Miyakawa T, Matsumoto T, Hisano S, Iijima K, Tranebjarg L, Shirahata A, Matsuo M, Kusuhara K.
- Journal Title
  
  Pediatr Nephrol 25(7)
  
  Pages: 1343-1348
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] Alport症候群と良性家族性血尿の遺伝子変異と臨床像"IV型コラーゲン関連腎症&cmp;quotという概念の提唱2010
- Author(s)
  田中幸代, 蓮井正史, 野津寛大, 飯島一誠, 杉本圭相, 竹村司, 金子一成
- Journal Title
  
  日本小児腎臓病学会雑誌
  
  Volume: 23 Pages: 172-178
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] HNF 1B Alterations Associated with Congenital Anomalies of the Kidney and Urinary Tract2010
- Author(s)
  Nakayama M, Nozu K, Goto Y, Kamei K, Ito S, Sato H, Emi M, Nakanishi K, Tuchiya S, Iijima K.
- Journal Title
  
  Pediatr Nephrol
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] A family with X-linked benign familial hematuria2010
- Author(s)
  Kaneko K, Tanaka S, Hasui M, Nozu K, Krol RP, Iijima K, Sugimoto K, Takemura T.
- Journal Title
  
  Pediatr Nephrol 25
  
  Pages: 545-548
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] Severe Alport syndrome in a young woman caused by a t(X;1)(q22.3;p36.32) balanced translocation2010
- Author(s)
  Iijima K, Nozu K, Kamei K, Nakayama M, Ito S, Matsuoka K, Ogata T, Kaito H, Nakanishi K, Matsuo M
- Journal Title
  
  Pediatr Nephrol
  
  Volume: 25 Pages: 2165-2170
- NAID
  120003307589
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] Severe Alport syndrome in a young woman caused by a t(X;1)(q22.3;p36.32) balanced translocation.2010
- Author(s)
  Iijima K, Nozu K, Kamei K, Nakayama M, Ito S, Matsuoka K, Ogata T, Kaito H, Nakanishi K, Matsuo M.
- Journal Title
  
  Pediatr Nephrol. 25(10)
  
  Pages: 2165-2170
- NAID
  120003307589
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article]2009
- Author(s)
  野津寛大, 飯島一誠
- Journal Title
  
  K[カリウム]『新しい小児の臨床検査基準値ポケットガイド』(田中敏章編)(じほう)
  
  Pages: 74-75
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] IPEX症候群と腎疾患2009
- Author(s)
  橋村裕也, 野津寛大, 神田杏子, 早川晶, 竹島泰弘, 金兼弘和, 宮脇利男, 飯島一誠, 松尾雅文
- Journal Title
  
  日本小児腎臓病学会雑誌 22
  
  Pages: 131-135
- NAID
  10026411780
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] Atypical phenotype of type I Bartter syndrome accompanied by focal segmental glomerulosclerosis.2009
- Author(s)
  Yamazaki H, Nozu K, Narita I, Nagata M, Nozu Y Fu XJ, Matsuo M, Iijima K, Gejyo F.
- Journal Title
  
  Pediatr Nephrol 24
  
  Pages: 415-418
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] Single dose of rituximab for refractory steroid-dependent nephrotic syndrome in children2009
- Author(s)
  Kamei K, Ito S, Nozu K, Fujinaga S, Nakayama M, Sako M, Saito M, Yoneko M, Iijima K.
- Journal Title
  
  Pediatr Nephrol 24
  
  Pages: 1321-1328
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] 偽性低アルドステロン症I型2009
- Author(s)
  神田杏子, 野津寛大, 橋村裕也, 飯島一誠, 松尾雅文
- Journal Title
  
  日本小児腎臓病学会雑誌 22
  
  Pages: 123-125
- NAID
  10026411765
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article]2009
- Author(s)
  野津寛大, 飯島一誠
- Journal Title
  
  Cl[クロール]『新しい小児の臨床検査基準値ポケットガイド』(田中敏章編)(じほう)
  
  Pages: 72-73
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] Increased chymase-positive mast cells in children with crescentic glomerulonephritis.2009
- Author(s)
  Togawa H, Nakanishi K, Shim a Y, Obana M, Sako M, Nozu K, Tanaka R, Iiiima K, Yoshikawa N.
- Journal Title
  
  Pediatr Nephrol (印刷中)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] A deep intronic mutation in the SLC12A3 gene leads to Gitelman syndrome2009
- Author(s)
  Nozu K, Iijima K, Nozu Y, Ikegami E, Imai T, Fu XJ, Kaito H, Nakanishi K, Yoshikawa N, Matsuo M.
- Journal Title
  
  Pediatr Res 66
  
  Pages: 590-593
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] 運動後急性腎不全(ALPE)を呈しPRES(Posterior Reversible Encephalopathy Syndrome)を合併した腎性低尿酸血症の1例2009
- Author(s)
  島友子, 中西浩一, 渋田昌一, 戸川寛子, 尾鼻美奈, 野津寛大, 貝藤裕史, 飯島一誠, 吉川徳茂
- Journal Title
  
  日本小児腎不全学会雑誌 29
  
  Pages: 120-121
- NAID
  10027866043
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] In vivo and in vitro splicing assay of SLC12A1 in an antenatal salt-losing tubulopathy patient with an intronic mutation2009
- Author(s)
  Nozu K, Iijima K, Kawai K, Nozu Y, Nishida A, Takeshima Y, Fu XJ, Hashimura Y, Kaito H, Nakanishi K, Yoshikawa N, Matsuo M.
- Journal Title
  
  Hum Genet 126
  
  Pages: 533-538
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] Detection by multiplex ligation-dependent probe amplification of largedeletion mutations in the COL4A5 gene in female patients with Alportsyndrome.2009
- Author(s)
  Nozu K, Krol RP Nakanishi K, Yoshikawa N, Nozu Y, Ohtsuka Y, Iijima K, Matsuo M.
- Journal Title
  
  Pediatr Nephrol (印刷中)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article]2009
- Author(s)
  野津寛大, 飯島一誠
- Journal Title
  
  Na[ナトリウム]『新しい小児の臨床検査基準値ポケットガイド』(田中敏章編)(じほう)
  
  Pages: 70-71
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] Autosomal dominant pseudohypoaldosteronism type 1 with a novel splice site mutation in MR gene.2009
- Author(s)
  Kanda K, Nozu K, Yokoyama N, Morioka I, Miwa A, Hashimura Y, Kaito H, Iijima K, Matsuo M.
- Journal Title
  
  BMC Nephrol 14
  
  Pages: 10-37
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] Increased chymase-positive mast cells in children with crescentic glomerulonephritis2009
- Author(s)
  Togawa H, Nakanishi K, Shima Y, Obana M, Sako M, Nozu K, Tanaka R, Iijima K, Yoshikawa N.
- Journal Title
  
  Pediatr Nephrol 24
  
  Pages: 1071-1075
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] In vivo and in vitro splicing assay of SLC12A1 in an antenatal salt-losing tubulopathy patient with an intronic mutation.2009
- Author(s)
  Nozu K, Iijima K, Kawai K, Nozu Y, Nishida A, Takeshima Y, Fu XJ, Hashimura Y, Kaito H, Nakanishi K, Yoshikawa N, Matsuo M.
- Journal Title
  
  Hum Genet 126(4)
  
  Pages: 533-538
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] 溶血性尿毒症症候群発症8年後より高度蛋白尿を呈し、糸球体硬化および著明な間質の線維化を認めた1例2009
- Author(s)
  橋村裕也, 野津寛大, 忍頂寺毅史, 貝藤裕史, 中西浩一, 吉川徳茂, 飯島一誠, 松尾雅文
- Journal Title
  
  日本小児腎臓病学会雑誌 22
  
  Pages: 183-187
- NAID
  10026411977
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] Detection by multiplex ligation-dependent probe amplification of large deletion mutations in the COL4A5 gene in female patients with Alport syndrome2009
- Author(s)
  Nozu K, Krol RP, Nakanishi K, Yoshikawa N, Nozu Y, Ohtsuka Y, Iijima K, Matsuo M.
- Journal Title
  
  Pediatr Nephrol (Epub ahead of print)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19790720
[Journal Article] Autosomal dominant pseudohypoaldosteronism type 1 with a novel splice site mutation in MR gene2009
- Author(s)
  Kyoko Kanda, Kandai Nozu, et al.
- Journal Title
  
  BMC nephrology 14
  
  Pages: 37-37
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21790986
[Journal Article] Minimal change nephrotic syndrome associated with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome2009
- Author(s)
  Hashimura Y, Nozu K, Kanegane H, Miyawaki T, Hayakawa A, Yoshikawa N, Nakanishi K, Takemoto M, Iijima K, Matsuo M.
- Journal Title
  
  Pediatr Nephrol 24
  
  Pages: 1181-1186
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] A deep intronic mutation in the SLC12A3 gene leads to Gitelman syndrome.2009
- Author(s)
  Nozu K, Iijima K, Nozu Y, Ikegami E, Imai T, Fu XJ, Kaito H, Nakanishi K, Yoshikawa N, Matsuo M.
- Journal Title
  
  Pediatr Res 66(5)
  
  Pages: 590-593
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] In vivo and in vitro splicing assay of SLC12A1 in an antenatal salt-losing tubulopathy patient with an intronic mutation2009
- Author(s)
  Kandai Nozu, et al.
- Journal Title
  
  Human Genetics 126
  
  Pages: 533-538
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21790986
[Journal Article] Membranous nephropathy associated with thyroid-peroxidase antigen.2009
- Author(s)
  Shima Y, Nakanishi K, Togawa H, Obana M, Sako M, Miyawaki M, Nozu K, Iijima K, Yoshikawa N.
- Journal Title
  
  Pediatr Nephrol 24
  
  Pages: 605-608
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] A Deep Intronic Mutation in the SLC12A3 Gene Leads to Gitelman Syndrome2009
- Author(s)
  Kandai Nozu, et al.
- Journal Title
  
  Pediatric Research 66
  
  Pages: 590-593
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-21790986
[Journal Article] Minimal change nephrotic syndrome associated with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome.2009
- Author(s)
  Hashimura Y, Nozu K, Kanegane H, Miyawaki T, Hayakawa A, Yoshikawa N, Nakanishi K, Takemoto M, Iijima K, Matsuo M.
- Journal Title
  
  Pediatr Nephrol 24(6)
  
  Pages: 1181-1186
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] Atypical phenotype of type I Bartter syndrome accompanied by focal segmental glomerulosclerosis.2009
- Author(s)
  Yamazaki H, Nozu K, Narita I, Nagata M, Nozu Y, Fu XJ, Matsuo M, Iijima K, Gejyo F.
- Journal Title
  
  Pediatr Nephrol 24(2)
  
  Pages: 415-418
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] Autosomal dominant pseudohypoaldosteronism type 1 with a novel splice site mutation in MR gene2009
- Author(s)
  Kanda K, Nozu K, Yokoyama N, Morioka I, Miwa A, Hashimura Y, Kaito H, Iijima K, Matsuo M.
- Journal Title
  
  BMC Nephrol 10
  
  Pages: 37-37
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] 当院にて2007年以降に経験した小児献腎移植の4例2009
- Author(s)
  兵頭洋二, 石村武志, 竹田雅, 貝藤裕史, 神田杏子, 野津寛大, 三宅秀明, 田中一志, 武中篤, 飯島一誠, 藤澤正人
- Journal Title
  
  日本小児腎不全学会雑誌 29
  
  Pages: 198-200
- NAID
  10027866233
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] Minimal change nephrotic syndrome associated with IPEX syndrome.2009
- Author(s)
  Hashimura Y, Nozu K, Kanegane H, Miyawaki T, Hayakawa A, Yoshikawa N, Nakanishi K, Takemoto M, Iiiima K, Matsuo M.
- Journal Title
  
  Pediatr Nephrol (印刷中)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] Detection of large deletion mutations in the COL4A5 gene of female Alport syndrome patients.2008
- Author(s)
  Nozu K, Przybyslaw Krol R, Ohtsuka Y, Nakanishi K, Yoshikawa N, Nozu Y, Kaito H, Kanda K, Hashimura Y, Hamasaki Y, Iiiima K, Matsuo M.
- Journal Title
  
  Pediatr Nephrol 23
  
  Pages: 2085-2090
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] Molecular analysis of digenic inheritance in Bartter syndrome with sensorineural deafness.2008
- Author(s)
  Nozu K, Inagaki T, Fu XJ, Nozu Y, Kaito H, Kanda K, Sekine T, Igarashi T, Nakanishi K, Yoshikawa N, Iijima K, Matsuo M.
- Journal Title
  
  J Med Genet 45
  
  Pages: 182-186
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] Molecular analysis of digenic inheritance in Bartter syndrome with sensorineural deafness2008
- Author(s)
  Nozu K
- Journal Title
  
  Journal of Medical Genetics (In press)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19790720
[Journal Article] Molecular analysis of digenic inheritance in Bartter syndrome with sensorineural deafness2008
- Author(s)
  Nozu K, Inagaki T, Fu XJ, Nozu Y, Kaito H, Kanda K, Sekine T, Igarashi T, Nakanishi K, Yoshikawa N, Iijima K, Matsuo M
- Journal Title
  
  J Med Genet 45
  
  Pages: 182-186
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19790720
[Journal Article] Molecular analysis of digenic inheritance in Bartter syndrome with sensorineural deafness.2008
- Author(s)
  Nozu, et.al.
- Journal Title
  
  J Med Genet 15
  
  Pages: 182-186
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19790720
[Journal Article] Somatic mosaicism for a mutation of the COL4A5 gene is a cause of mild phenotype male Alport syndrome.2008
- Author(s)
  Krol RP, Nozu K, Nakanishi K, Iijima K, Takeshima Y, Fu XJ, Nozu Y, Kaito H, Kanda K, Matsuo M, Yoshikawa N.
- Journal Title
  
  Nephrol Dial Transplant. 23(8)
  
  Pages: 2525-3250
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] Diverse splicing abnormality caused by a homozygous mutation in the thiazide-sensitive sodiumchloride cotransporter gene in a patient with Gitelman's syndrome2008
- Author(s)
  Iida K, Nozu K, Takahashi Y, Okimura Y, Kaji H, Matsuo M, Chihara K.
- Journal Title
  
  Am J Kidney Dis 51
  
  Pages: 1077-1078
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19790720
[Journal Article] Improved renal survival in Japanese children with IgA nephropathy.2008
- Author(s)
  Yata N, Nakanishi K, Shima Y, Togawa H, Obana M, Sako M, Nozu K, Tanaka R, Iijima K, Yoshikawa N
- Journal Title
  
  Pediatr Nephrol 23
  
  Pages: 905-912
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] Detection of large deletion mutations in the COL4A5 gene of female Alport syndrome patients2008
- Author(s)
  Nozu K, Przybyslaw Krol R, Ohtsuka Y, Nakanishi K, Yoshikawa N, Nozu Y, Kaito H, Kanda K, Hashimura Y, Hamasaki Y, Iijima K, Matsuo M.
- Journal Title
  
  Pediatr Nephrol 23
  
  Pages: 2085-2090
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19790720
[Journal Article] Detection of large deletion mutations in the COL4A5 gene of female Alport syndrome patients.2008
- Author(s)
  Nozu K, Przybyslaw Krol R, Ohtsuka Y, Nakanishi K, Yoshikawa N, Nozu Y, Kaito H, Kanda K, Hashimura Y, Hamasaki Y, Iijima K, Matsuo M.
- Journal Title
  
  Pediatr Nephrol. 23(11)
  
  Pages: 2085-2090
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] Risk factors for developing severe clinical course in HUS patients : a national survey in Japan.2008
- Author(s)
  Kamioka I, Yoshiya K, Satomura K, Kaito H, Fujita T, Iijima K, Nakanishi K, Yoshikawa N, Nozu K, Matsuo M; Japanese Society for Pediatric Nephrology.
- Journal Title
  
  Pediatr Int 50
  
  Pages: 441-446
- NAID
  10025344153
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] Atypical phenotype of type I Bartter syndrome accompanied by focal segmental glomerulosclerosis2008
- Author(s)
  Yamazaki H, Nozu K, Narita I, Nagata M, Nozu Y, Fu XJ, Matsuo M, Iijima K, Gejyo F.
- Journal Title
  
  Pediatr Nephrol (Epub ahead of print)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19790720
[Journal Article] Oxidative imbalance in idiopathic renal hypouricemia2008
- Author(s)
  Kaneko K, Taniguchi N, Tanabe Y, Nakano T, Hasui M, Nozu K.
- Journal Title
  
  Pediatr Nephrol (Epub ahead of print)
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19790720
[Journal Article] Somatic mosaicism for a mutation of the COL4A5 gene is a cause of mild phenotype male Alport syndrome2008
- Author(s)
  Krol RP, Nozu K, Nakanishi K, Iijima K, Takeshima Y, Fu XJ, Nozu Y, Kaito H, Kanda K, Matsuo M, Yoshikawa N.
- Journal Title
  
  Nephrol Dial Transplant 23(8)
  
  Pages: 2525-2530
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19790720
[Journal Article] Somatic mosaicism for a mutation of the COL4A5 gene is a cause of mild phenotype male Alport syndrome.2008
- Author(s)
  Krol RP, Nozu K, Nakanishi K, Iiiima K, Takeshima Y, Fu XJ, Nozu Y, Kaito H, Kanda K, Matsuo M, Yoshikawa N.
- Journal Title
  
  Nephrol Dial Transplant 23
  
  Pages: 2525-2530
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390240
[Journal Article] OCRL1 mutations in patients with Dent phenotype in Japan. Pediatr Nephrol2007
- Author(s)
  Sekine T, Nozu K, Iyengar R, Fu XJ, Matsuo M, Tanaka R, Iijima K, Matsui M, Harita Y, Inatomi J, Igarashi T
- Journal Title
  
  22
  
  Pages: 975-980
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19790720
[Journal Article] Detection of a transcript abnormality in mRNA of the SLC12A3 gene extracted from urinary sediment cells of a patient with Gitelman's syndrome2007
- Author(s)
  Kaito H, Nozu K, Fu XJ, Kamioka I, Fujita T, Kanda K, Krol RP, Suminaga R, Ishida A, Iijima K, Matsuo M
- Journal Title
  
  Pediatric Research 61(4)
  
  Pages: 502-505
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19790720
[Journal Article] A novel mutation in KCNJ1 in a Bartter syndrome case diagnosed as pseudohyp oaldosteronism2007
- Author(s)
  Nozu K
- Journal Title
  
  Pediatric Nephrology 22
  
  Pages: 1219-23
- NAID
  120000943595
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19790720
[Journal Article] Molecular Analysis of Patients With Type III Bartter Syndrome : Picking Up Large Heterozygous Deletions With Semiquantitative PCR2007
- Author(s)
  Nozu K, Fu XJ, Nakanishi K, Yoshikawa N, Kaito H, Kanda K, Krol RP, Miyashita R, Kamitsuji H, Kanda S, Hayashi Y, Satomura K, Shimizu N, Iijima K, Matsuo M.
- Journal Title
  
  Pediatr Res 62
  
  Pages: 364-369
- NAID
  10025701181
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19790720
[Journal Article] A novel mutation in KCNJ1 in a Bartter syndrome case diagnosed as pseudohypoaldosteronism2007
- Author(s)
  Nozu K, Fu XJ, Kaito H, Kanda K, Yokoyama N, Krol PR, Nakajima T, Kajiyama M, Iijima K, Matsuo M
- Journal Title
  
  Pediatr Nephrol 22
  
  Pages: 1219-1223
- NAID
  120000943595
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19790720
[Journal Article] Molecular Analysis of Patients With Type III Bartter Syndrome: Picking Up Lar ge Heterozygous Deletions With Semiquantitative PCR2007
- Author(s)
  Nozu K
- Journal Title
  
  Pediatric Nephrology 62
  
  Pages: 364-9
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-19790720
[Journal Article] A novel mutation in KCNJ1 in a Bartter syndrome case diagnosed as pseudohypoaldosteronism2007
- Author(s)
  Nozu K
- Journal Title
  
  Pediatric Nephrology (In press)
- NAID
  120000943595
- Data Source
  KAKENHI-PROJECT-17790704
[Journal Article] Gitelman症候群2007
- Author(s)
  野津寛大
- Journal Title
  
  小児腎臓学会雑誌 (印刷中)
- Data Source
  KAKENHI-PROJECT-17790704
[Journal Article] Bartter症候群の表現型、遺伝子型の相関2006
- Author(s)
  野津寛大
- Journal Title
  
  Annual review 2006腎臓 2006
  
  Pages: 180-189
- Data Source
  KAKENHI-PROJECT-17790704
[Journal Article] Bartter症候群の表現型、遺伝子型の相関2006
- Author(s)
  野津寛大
- Journal Title
  
  Annual Review 腎臓 2006
  
  Pages: 180-189
- Data Source
  KAKENHI-PROJECT-17790704
[Journal Article] Bartter症候群2006
- Author(s)
  野津寛大
- Journal Title
  
  腎と透析 vol61 No6
  
  Pages: 835-840
- NAID
  10029736462
- Data Source
  KAKENHI-PROJECT-17790704
[Journal Article] Severe Alport syndrome in a female caused by a t(X;1)(q22.3;p36.32)balanced translocation
- Author(s)
  Iijima K, Nozu K, Kamei K, Nakayama K, Ito S, Natsuoka K, Ogata T, Kaito H, Nakanishi K, Matsuo M.
- Journal Title
  
  Pediatr Nephrol (In press(掲載確定))
- Peer Reviewed
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] OCRL異常症の表現型は、phosphatidylinositol 4,5-bisphosphate 5-phosphatase活性と相関する2024
- Author(s)
  鈴木諒太、榊原菜々、市川裕太、北角英晶、上田知佳、田中悠、近藤淳、長野智那、堀之内智子、岡本孝之、野津寛大
- Organizer
  日本小児腎臓病学会
- Data Source
  KAKENHI-PROJECT-23K07310
[Presentation] 早産や低出生体重児の潜在的レニン・アンギオテンシン・アルドステロン（RAAS）系亢進の存在に関する検討2024
- Author(s)
  石森真吾、北角英晶、近藤淳、藤村順也、堀之内智子、野津寛大
- Organizer
  第67回　日本腎臓学会学術集会
- Data Source
  KAKENHI-PROJECT-23K07242
[Presentation] OCRL異常症の表現型は、phosphatidylinositol 4,5-bisphosphate 5-phosphatase活性と相関する2024
- Author(s)
  鈴木諒太、榊原菜々、市川裕太、北角英晶、上田知佳、田中悠、近藤淳、長野智那、堀之内智子、岡本孝之、野津寛大
- Organizer
  日本腎臓学会
- Data Source
  KAKENHI-PROJECT-23K07310
[Presentation] 早産や低出生体重児の潜在的レニン・アンギオテンシン・アルドステロン系亢進の存在に関する検討2024
- Author(s)
  石森真吾、北角英晶、近藤淳、藤村順也、堀之内智子、野津寛大
- Organizer
  第59回　日本小児腎臓病学会学術集会
- Data Source
  KAKENHI-PROJECT-23K07242
[Presentation] 小児科医が知っておかなければならない分子生物学的観点から見た腎臓の機能と構造2024
- Author(s)
  野津寛大
- Organizer
  第127回日本小児科学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-23K07698
[Presentation] Onset mechanisms and prognosis in pediatric patients with IgA nephropathy accompanied by macrohematuria-induced acute kidney injury: a multicenter study2023
- Author(s)
  Shingo Ishimori, Tomoko Horinouchi, Tomohiko Yamamura, Junya Fujimura, Naohiro Kamiyoshi, Hiroshi Kaito, Yuriko Tanaka, Hiroki Matsukura, Wataru Shimabukuro, Yuko Shima, Azusa Kawaguchi, Yoshinori Araki, Koichi Nakanishi, Shigeo Hara, Kandai Nozu
- Organizer
  15th Asian Congress of Pediatric Nephrology
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-23K07242
[Presentation] Holistic Approach to Diagnosing and Treating Genetic Kidney Diseases.2023
- Author(s)
  Kandai Nozu
- Organizer
  The 13 th Chronic Kidney Disease Frontier Meeting
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-23K07698
[Presentation] 4型コラーゲン関連腎症の発症機序と核酸医薬を用いたエクソンスキッピング療法の開発2021
- Author(s)
  野津寛大
- Organizer
  第53回日本結合組織学会
- Invited
- Data Source
  KAKENHI-PROJECT-19K08726
[Presentation] 遺伝性腎疾患研究最前線：国内で行われている最先端の研究に触れる2021
- Author(s)
  野津寛大
- Organizer
  第64回日本腎臓学会学術総会
- Invited
- Data Source
  KAKENHI-PROJECT-19K08726
[Presentation] Bartter syndrome and Gitelman syndrome2021
- Author(s)
  Kandai Nozu
- Organizer
  14th Asian Congress of Pediatric Nephrology
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K08726
[Presentation] Participation in "KDIGO in Genetics" working group as a researcher2021
- Author(s)
  野津寛大
- Organizer
  第64回日本腎臓学会学術総会
- Invited
- Data Source
  KAKENHI-PROJECT-19K08726
[Presentation] 14.Novel Exon Skipping therapy in Alport’s Syndrome to prevent CKD and ESRD2021
- Author(s)
  Kandai Nozu
- Organizer
  9th Annual Emerging Trands in Dialysis Care
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K08726
[Presentation] 小児ネフローゼ症候群の病因探索研究および治療開発研究 UP TO Date2021
- Author(s)
  飯島一誠、野津寛大、佐古まゆみ
- Organizer
  第55回日本小児腎臓病学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-20H03698
[Presentation] Bartter syndrome and Gitelman syndrome2021
- Author(s)
  Nozu K
- Organizer
  14th Asian Congress of Pediatric Nephrology
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K08726
[Presentation] Alport syndrome Up To Date and development of gene targeted therapy2020
- Author(s)
  Nozu K
- Organizer
  Korean Society of Nephrology, virtual meeting
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K08726
[Presentation] Exon skipping therapy in Alport syndrome2020
- Author(s)
  Nozu K
- Organizer
  The American Society of Nephrology Annual Meeting
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K08726
[Presentation] 遺伝性腎疾患に対するプレシジョンメディスン　アルポート症候群に対する遺伝子標的療法の開発2019
- Author(s)
  野津寛大、山村智彦、飯島一誠
- Organizer
  第54回日本小児腎臓病学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-17H04189
[Presentation] 常染色体劣性Alport症候群39家系46人の臨床遺伝学的検討2019
- Author(s)
  堀之内智子、野津寛大、榊原菜々、長野智那、南川将吾、山村智彦、飯島一誠
- Organizer
  第62回日本腎臓学会学術集会
- Data Source
  KAKENHI-PROJECT-17H04189
[Presentation] これからの小児科学研究をどのように進めるか；活躍する先輩小児科physician-scientistからのメッセ－ジ2019
- Author(s)
  野津寛大
- Organizer
  第122回日本小児科学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-19K08726
[Presentation] 遺伝性腎疾患に対するプレシジョンメディスン　アルポート症候群に対する遺伝子標的療法の開発2019
- Author(s)
  野津寛大
- Organizer
  第54回日本小児腎臓病学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-19K08726
[Presentation] 遺伝性腎疾患に対するプレシジョンメデイスン　小児ステロイド感受性ネフローゼ症候群の疾患感受性遺伝子2019
- Author(s)
  飯島一誠、 Jia Xiaoyuan,、山村智彦、人見祐基、長野智那、堀之内智子、野津寛大、徳永勝士
- Organizer
  第54回日本小児腎臓病学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-18KK0244
[Presentation] ゲノムから見た腎臓病　症例から考える遺伝性尿細管疾患2019
- Author(s)
  野津寛大
- Organizer
  第62回日本腎臓学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-19K08726
[Presentation] Alport症候群モデルマウスにおけるエクソンスキッピング療法の有効性の検討2019
- Author(s)
  山村智彦、野津寛大、堀之内智子、南川将吾、足立朝美、寺川真紀、永瀬弘之、高石巨澄、大西朗之、小路貴生、小泉誠、神田祥一郎、張田豊、嘉村美里、甲斐広文、飯島一誠
- Organizer
  第54回日本小児腎臓病学会学術集会
- Data Source
  KAKENHI-PROJECT-17H04189
[Presentation] 9.Genetics and development of exon-skipping therapy for Alport Syndrome.2019
- Author(s)
  Kandai Nozu
- Organizer
  International Pediartic Nephrology Association 2019
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K08726
[Presentation] Bartter syndrome2019
- Author(s)
  Kandai Nozu
- Organizer
  International Pediartic Nephrology Association 2019
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-19K08726
[Presentation] 遺伝性ネフローゼ症候群における臨床的特徴の検討2019
- Author(s)
  長野智那、野津寛大、青砥悠哉、石河慎也、榊原菜々、南川将吾、山村智彦、飯島一誠
- Organizer
  第54回日本小児腎臓病学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-18KK0244
[Presentation] Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome2019
- Author(s)
  Tomoko Horinouchi, Tomohiko Yamamura, Rasheed A. Gbadegesin, Matthew G. Sampson, China Nagano, Kandai Nozu, Kenji Ishikura, Pierre M. Ronco, Hae Il Cheong, Kazumoto Iijima
- Organizer
  American Society of Nephrology Kidney week 2019
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-18KK0244
[Presentation] Exon skipping therapy for COL4A5 gene truncating variant rescued progression of kidney failure in X-linked Alport syndrome2019
- Author(s)
  Tomohiko Yamamura, Kandai Nozu, Kazumoto Iijima
- Organizer
  American Society of Nephrology Kidney week 2019
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17H04189
[Presentation] NPHS1は小児ステロイド感受性ネフローゼ症候群の疾患感受性遺伝子である2019
- Author(s)
  山村智彦、長野智那、堀之内智子、野津寛大、飯島一誠
- Organizer
  第62回日本腎臓学会学術集会
- Data Source
  KAKENHI-PROJECT-18KK0244
[Presentation] 先天性/乳児およびステロイド抵抗性ネフローゼ症候群における網羅的遺伝子診断2019
- Author(s)
  長野智那、野津寛大、青砥悠哉、石河慎也、榊原菜々、南川将吾、山村智彦、飯島一誠
- Organizer
  第122回日本小児科学会学術集会
- Data Source
  KAKENHI-PROJECT-18KK0244
[Presentation] 常染色体劣性Alport症候群39家系46人の臨床遺伝学的検討2019
- Author(s)
  堀之内智子、野津寛大、石河慎也、青砥悠哉、榊原菜々、長野智那、南川将吾、山村智彦、貝藤裕史、森貞直哉、飯島一誠
- Organizer
  第54回日本小児腎臓病学会学術集会
- Data Source
  KAKENHI-PROJECT-17H04189
[Presentation] Factors regulating the severity in male X-linked Alport syndrome: study of 367 cases2018
- Author(s)
  Yamamura T, Nozu K, Sakakibara N, Nagano C, Fujimura J, Horinouchi T, Nakanishi K, Minamikawa S, Kaito H, Shima Y, Nakanishi K, Iijima K
- Organizer
  52st Annual Meeting of the American Society of Nephrology
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17H04189
[Presentation] 次世代シークエンサーを用いたAlport症候群の網羅的診断法の確立2018
- Author(s)
  山村　智彦、野津　寛大、長野　智那、榊原　菜々、藤村　順也、堀之内　智子、中西　啓太、南川　将吾、貝藤　裕史、飯島　一誠
- Organizer
  第121回日本小児科学会学術集会
- Data Source
  KAKENHI-PROJECT-17H04189
[Presentation] ゲノムワイド関連解析による小児特発性ネフローゼ症候群のrisk haplotype同定2018
- Author(s)
  堀之内　智子、野津　寛大、石倉　健司、飯島　一誠
- Organizer
  第61回日本腎臓学会学術総会
- Data Source
  KAKENHI-PROJECT-18KK0244
[Presentation] ネフローゼ症候群の病因としての遺伝子異常2018
- Author(s)
  野津　寛大、中西　啓太、飯島　一誠
- Organizer
  第53回小児腎臓病学会学術集会
- Data Source
  KAKENHI-PROJECT-18KK0244
[Presentation] ゲノムワイド関連解析による小児特発性ネフローゼ症候群のrisk haplotype同定2018
- Author(s)
  堀之内　智子、Xiaoyuan Jia、人見　祐基、石倉　健司、亀井　宏一、濱田　陸、郭　義胤、藤丸　季可、岡本　孝之、大和田　葉子、田中　亮二郎、後藤　芳充、貝籐　裕史、野津　寛大、徳永　勝士、飯島　一誠
- Organizer
  第53回小児腎臓病学会学術集会
- Data Source
  KAKENHI-PROJECT-18KK0244
[Presentation] X染色体連鎖型Alport症候群男性患者341名の臨床遺伝学的検討2018
- Author(s)
  山村　智彦、野津　寛大、榊原　菜々、長野　智那、藤村　順也、堀之内　智子、中西　啓太、南川　将吾、貝藤　裕史、中西　浩一、飯島　一誠
- Organizer
  第61回日本腎臓学会学術総会
- Data Source
  KAKENHI-PROJECT-17H04189
[Presentation] Genotype-phenotype correlation in male X-linked Alport syndrome: 341 cases study2018
- Author(s)
  Yamamura T, Sakakibara N, Nagano C, Nozu K, Fujimura J, Horinouchi T, Nakanishi K, Minamikawa S, Kaito H, Iijima K
- Organizer
  第53回小児腎臓病学会学術集会
- Data Source
  KAKENHI-PROJECT-17H04189
[Presentation] Splicing assay with hybrid minigene: assessing pathogenicities in COL4A5 intronic mutations2018
- Author(s)
  Horinouchi T, Nozu K, Yamamura T, Sakakibara N, Nagano C, Nakanishi K, Fujimura J, Minamikawa S, Ninchoji T, Kaito H, Shima Y, Nakanishi K, Iijima K
- Organizer
  52st Annual Meeting of the American Society of Nephrology
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17H04189
[Presentation] 尿細管機能異常と電解質2017
- Author(s)
  野津寛大
- Organizer
  第7回東北小児内分泌講演会
- Invited
- Data Source
  KAKENHI-PROJECT-15K09691
[Presentation] 次世代シークエンサーを用いたAlport症候群の網羅的診断法の確立2017
- Author(s)
  山村智彦、野津寛大、藤村順也、堀之内智子、中西啓太、南川将吾、庄野朱美、忍頂寺毅史、貝藤裕史、中西浩一、飯島一誠
- Organizer
  第60回日本腎臓学会　仙台
- Data Source
  KAKENHI-PROJECT-17H04189
[Presentation] エクソンスキッピング療法によるアルポート症候群特異的療法治療法の開発2017
- Author(s)
  庄野朱美、野津寛大、小泉　誠、大西朗之、高石巨澄、山村智彦、南川将吾、飯島一誠
- Organizer
  第52回日本小児腎臓病学会　東京
- Data Source
  KAKENHI-PROJECT-17H04189
[Presentation] Establishment of a comprehensive　diagnostic method using next generation sequencer for the Alport syndrome2017
- Author(s)
  Yamamura T, Nozu K, Fujimura J, Horinouchi T, Nakanishi K, Manamikawa S, Shono A, Ninchoji T, Kaito H, Nakanishi K, Iijima K
- Organizer
  第52回日本小児腎臓病学会　東京
- Data Source
  KAKENHI-PROJECT-17H04189
[Presentation] A comprehensive diagnosis by targeted sequencing for clinically suspectsd alport syndrome patients in Japan2017
- Author(s)
  Yamamura T, Nozu K, Fujimura J, Horinouchi T, Nakanishi K, Minamikawa S, Shono A, Ninchoji T, Kaito H, Shima Y, Nakanishi K, Iijima K.
- Organizer
  Asian Congress of Pediatric Nephrology 2017 & 39th Malaysian Pediatric Association Annual Congress, Kuala Lumpur, Malaysia
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-17H04189
[Presentation] 次世代シークエンサーを用いたAlport症候群の網羅的診断法の確立2017
- Author(s)
  山村智彦、野津寛大、藤村順也、堀之内智子、中西啓太、南川将吾、庄野朱美、忍頂寺毅史、貝藤裕史、中西浩一、飯島一誠
- Organizer
  第60回日本腎臓学会　仙台
- Data Source
  KAKENHI-PROJECT-26293203
[Presentation] A comprehensive diagnosis by targeted sequencing for clinically suspectsd alport syndrome patients in Japan2017
- Author(s)
  Yamamura T, Nozu K, Fujimura J, Horinouchi T, Nakanishi K, Minamikawa S, Shono A, Ninchoji T, Kaito H, Shima Y, Nakanishi K, Iijima K.
- Organizer
  Asian Congress of Pediatric Nephrology 2017 & 39th Malaysian Pediatric Association Annual Congress, Kuala Lumpur, Malaysia
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26293203
[Presentation] 遺伝性腎疾患の研究から学んだ大切なこと－研究の楽しさと臨床へのフィードバック－2017
- Author(s)
  野津寛大
- Organizer
  第120回日本小児科学会学術集会
- Invited
- Data Source
  KAKENHI-PROJECT-15K09691
[Presentation] エクソンスキッピング療法によるアルポート症候群特異的療法治療法の開発2017
- Author(s)
  庄野朱美、野津寛大、小泉　誠、大西朗之、高石巨澄、山村智彦、南川将吾、飯島一誠
- Organizer
  第52回日本小児腎臓病学会　東京
- Data Source
  KAKENHI-PROJECT-26293203
[Presentation] Establishment of a comprehensive　diagnostic method using next generation sequencer for the Alport syndrome2017
- Author(s)
  Yamamura T, Nozu K, Fujimura J, Horinouchi T, Nakanishi K, Manamikawa S, Shono A, Ninchoji T, Kaito H, Nakanishi K, Iijima K
- Organizer
  第52回日本小児腎臓病学会　東京
- Data Source
  KAKENHI-PROJECT-26293203
[Presentation] Genetic and clinical characteristics of female X-linked Alport Syndrome: 267case study2016
- Author(s)
  Yamamura T, Nozu K, Nakanishi K, Horinouchi T, Fujimura J, Minamikawa S, Kamiyoshi N, Ninchoji T, Kaito H, Morisada N, Nakanishi K, Yoshikawa N, Iijima K
- Organizer
  17th Congress of the International Pediatric Nephrology Association
- Place of Presentation
  RAFAIN PALACE HOTEL & CONVENTION (Iguazu, Brazil)
- Year and Date
  2016-09-20
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26293203
[Presentation] 特発性ネフローゼ症候群の成因と治療2016
- Author(s)
  野津寛大
- Organizer
  第52回日本小児腎臓病学会学術集会
- Place of Presentation
  名古屋
- Year and Date
  2016-07-07
- Invited
- Data Source
  KAKENHI-PROJECT-15K09691
[Presentation] 男女共同参画委員会企画：遺伝性腎疾患2016
- Author(s)
  野津寛大,　森貞直哉,　飯島一誠
- Organizer
  第59回日本腎臓学会学術総会
- Place of Presentation
  パシフィコ横浜（横浜）
- Year and Date
  2016-06-17
- Invited
- Data Source
  KAKENHI-PROJECT-26293203
[Presentation] ネフローゼ症候群と遺伝子-どこまで分かっているか、どのような場合遺伝子診断が必要か2016
- Author(s)
  野津寛大
- Organizer
  第52回日本小児腎臓病学会学術集会
- Place of Presentation
  名古屋
- Year and Date
  2016-07-07
- Invited
- Data Source
  KAKENHI-PROJECT-15K09691
[Presentation] Gene targeting therapy for Alport syndrome2016
- Author(s)
  Kandai Nozu
- Organizer
  2016 Pediatric Academic Societies Meeting
- Place of Presentation
  Baltimore
- Year and Date
  2016-05-02
- Invited / Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-15K09691
[Presentation] 次世代シークエンサーによる染色体優性Alport症候群診断法の確立2016
- Author(s)
  神吉直宙,　野津寛大, 中西啓太,　堀之内智子,　藤村順也,　南川将吾,　山村智彦　松野下夏樹,　忍頂寺毅史,　飯島一誠
- Organizer
  第119回日本小児科学会学術集会
- Place of Presentation
  ロイトン札幌（札幌）
- Year and Date
  2016-05-13
- Data Source
  KAKENHI-PROJECT-26293203
[Presentation] 次世代シークエンサー（NGS）による染色体優性Alport症候群診断法の確立および臨床的、病理学的検討2016
- Author(s)
  山村智彦,　野津寛大,　南川将吾,　神吉直宙,　忍頂寺毅史,　飯島一誠
- Organizer
  第59回日本腎臓学会学術総会
- Place of Presentation
  パシフィコ横浜（横浜）
- Year and Date
  2016-06-17
- Data Source
  KAKENHI-PROJECT-26293203
[Presentation] X染色体連鎖型Alport症候群女性267例の遺伝学的・臨床的検討2016
- Author(s)
  山村智彦, 野津寛大, 中西啓太, 堀之内智子, 藤村順也, 南川将吾,　神吉直宙, 忍頂寺毅史, 貝藤裕史, 森貞直哉, 中西浩一, 吉川徳茂, 飯島一誠
- Organizer
  第51回日本小児腎臓病学会学術集会
- Place of Presentation
  ウインクあいち（名古屋）
- Year and Date
  2016-07-07
- Data Source
  KAKENHI-PROJECT-26293203
[Presentation] 男女共同参画「genderと腎-遺伝性腎疾患」2016
- Author(s)
  野津寛大、飯島一誠
- Organizer
  第60回日本腎臓学会
- Place of Presentation
  東京
- Year and Date
  2016-06-18
- Invited
- Data Source
  KAKENHI-PROJECT-15K09691
[Presentation] ターゲットシークエンス法による常染色体優性Alport症候群診断法の確立および遺伝学的背景、臨床的、病理学的検討2016
- Author(s)
  神吉直宙、野津寛大、中西啓太、堀之内智子、藤村順也、南川将吾、　山村智彦、松野下夏樹、忍頂寺毅史、中西浩一、吉川徳茂、飯島一誠
- Organizer
  第51回日本小児腎臓病学会学術集会
- Place of Presentation
  ウインクあいち（名古屋）
- Year and Date
  2016-07-07
- Data Source
  KAKENHI-PROJECT-26293203
[Presentation] 教育講演　小児腎疾患診療における遺伝学的アプローチ2015
- Author(s)
  飯島一誠，森貞直哉，野津寛大
- Organizer
  第37回日本小児腎不全学会学術集会
- Place of Presentation
  石川
- Year and Date
  2015-11-26
- Invited
- Data Source
  KAKENHI-PROJECT-26293203
[Presentation] 常染色体優性Alport症候群の遺伝学的背景と臨床像2015
- Author(s)
  神吉直宙，野津寛大，南川将吾，山村智彦，松野下夏樹，大坪裕美，忍頂寺毅史，貝藤裕史，飯島一誠
- Organizer
  第58回日本腎臓学会学術総会
- Place of Presentation
  名古屋
- Year and Date
  2015-06-05
- Data Source
  KAKENHI-PROJECT-26293203
[Presentation] Genetic, pathological and clinical backgrounds in autosomal dominant Alport syndrome.2015
- Author(s)
  Nozu K, Kamiyoshi N, Matsunoshita N, Minamikawa S, Yamamura T, Ninchoji T, Tanaka R, Nakanishi K, Yoshikawa N, Iijima K.
- Organizer
  48th Annual Scientific Meeting of the European Society for Pediatric Nephrology
- Place of Presentation
  Square Brussels Meeting Centre (Brussels, Belgium)
- Year and Date
  2015-09-03
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26293203
[Presentation] 常染色体優性Alport症候群における遺伝学的背景および臨床的、病理学的検討2015
- Author(s)
  神吉直宙，野津寛大，南川将吾，山村智彦，松野下夏樹，大坪裕美，忍頂寺毅史，貝藤裕史，飯島一誠
- Organizer
  日本小児腎臓病学会学術集会　第50回記念大会
- Place of Presentation
  神戸
- Year and Date
  2015-06-18
- Data Source
  KAKENHI-PROJECT-26293203
[Presentation] ワークショップ１　腎炎・ネフローゼ症候群の治療トピックス　難治性ネフローゼ症候群に対するリツキシマブ治療2015
- Author(s)
  飯島一誠，野津寛大，佐古まゆみ
- Organizer
  第45回日本腎臓学会西部学術大会
- Place of Presentation
  金沢
- Year and Date
  2015-10-23
- Invited
- Data Source
  KAKENHI-PROJECT-26293203
[Presentation] Somatic Mosaicism and Variant Frequency Detected by Next Generation Sequencing in X Linked Alport Syndrome.2015
- Author(s)
  Kamiyoshi N, Nozu K, Fu X.J, Yamamura T, Minamikawa S, Ninchoji T, Iijima K.
- Organizer
  Kidney Week 2015
- Place of Presentation
  San Diego Convention Center (San Diego, U.S.A.)
- Year and Date
  2015-11-03
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26293203
[Presentation] Comprehensive Approach to Understand Human Renal Development Based on the Identification of Responsible Genes for CAKUT.2015
- Author(s)
  Shono A, Morisada N, Nozu K, Iijima K.
- Organizer
  Kidney Week 2015
- Place of Presentation
  San Diego Convention Center (San Diego, U.S.A.)
- Year and Date
  2015-11-03
- Int'l Joint Research
- Data Source
  KAKENHI-PROJECT-26293203
[Presentation] 遺伝子解析で確定診断しえたGitelman症候群31例の臨床的検討2010
- Author(s)
  貝藤裕史、野津寛大、橋村裕也、岡政史、忍頂寺毅史、飯島一誠、松尾雅文
- Organizer
  第45回日本小児腎臓病学会学術集会
- Place of Presentation
  大阪国際会議場(大阪府)
- Year and Date
  2010-07-02
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] Clinical Characteristics of Genetically-Proven Gitelman's Syndrome2010
- Author(s)
  Kaito H,Nozu N,Hashimura Y,Oka M,Ninchoji T,Nakanishi K,Yoshikawa N,Iijima K,Matsuo M
- Organizer
  the 15th Congress of the International Pediatric Nephrology Association
- Place of Presentation
  New York Hilton(アメリカ)
- Year and Date
  2010-08-29
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] 3歳健診から血尿と蛋白尿が持続し,Alport症候群の孤発例と考えられた女児例2010
- Author(s)
  海野杏奈、沢登恵美、松下香子、東田耕輔、杉田完爾、野津寛大、Krol Rafal P、飯島一誠
- Organizer
  第113回日本小児科学会学術集会
- Place of Presentation
  いわて県民情報交流センター(岩手県)
- Year and Date
  2010-04-25
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] X染色体連鎖型Alport症候群と血友病Aを合併した一男児例-同胞男児間における表現型の差異についての分子遺伝学的検討-2010
- Author(s)
  橋村裕也、野津寛大、岡政史、忍頂寺毅史、貝藤裕史、飯島一誠、松尾雅文
- Organizer
  第45回日本小児腎臓病学会学術集会
- Place of Presentation
  大阪国際会議場(大阪府)
- Year and Date
  2010-07-02
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] Epithelial-to-Mesenchymal Transition(EMT)in cpk Mouse, a Model of ARPKD2010
- Author(s)
  Togawa H, Nakanishi K, Mukaiyama H, Hama T, Shima Y, Miyajima M, Nozu K, Takahashi H, Nagao S,Iijima K, Yoshikawa N
- Organizer
  Renal Week 2010
- Place of Presentation
  Colorado Convention Center(アメリカ)
- Year and Date
  2010-11-16
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] 伴性優性遺伝の家族性良性血尿の1家系2010
- Author(s)
  田中幸代、蓮井正史、野津寛大、飯島一誠、杉本圭相、竹村司、金子一成
- Organizer
  第45回日本小児腎臓病学会学術集会
- Place of Presentation
  大阪国際会議場(大阪府)
- Year and Date
  2010-07-02
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] 運動後急性腎不全とPRESの合併を反復し、GLUT9遺伝子複合ヘテロ接合体変異を同定しえた腎性低尿酸血症の一例2010
- Author(s)
  島友子、野津寛大、戸川寛子、貝藤裕史、飯島一誠、松尾雅文、中西浩一、吉川徳茂
- Organizer
  第45回日本小児腎臓病学会学術集会
- Place of Presentation
  大阪国際会議場(大阪府)
- Year and Date
  2010-07-02
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] 微小変化・巣状メサンギウム増殖を示す小児IgA腎症における自然寛解率とその予測因子2010
- Author(s)
  島友子、中西浩一、戸川寛子、野津寛大、田中亮二郎、飯島一誠、吉川徳茂
- Organizer
  第45回日本小児腎臓病学会学術集会
- Place of Presentation
  大阪国際会議場(大阪府)
- Year and Date
  2010-07-02
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] 幼少期発症のFibronectin腎症でFN1遺伝子に変異のあった1例2010
- Author(s)
  川西智子、笠原正登、森潔、横井秀基、桑原孝成、城謙輔、上杉憲子、長田道夫、野津寛大、飯島一誠、向山政志、中尾一和
- Organizer
  第40回日本腎臓学会西部学術大会
- Place of Presentation
  広島国際会議場(広島県)
- Year and Date
  2010-10-08
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] 多嚢胞性異形成腎(MCDK)の兄弟例におけるHNF-1β遺伝子変異2010
- Author(s)
  蓮井正史、磯崎夕佳、田中幸代、金子一成、野津寛大、飯島一誠
- Organizer
  第45回日本小児腎臓病学会学術集会
- Place of Presentation
  大阪国際会議場(大阪府)
- Year and Date
  2010-07-02
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] COL4A3/COL4A4のヘテロ変異を有する菲薄基底膜症候群のドナーから腎移植を実施した2例2010
- Author(s)
  梶保祐子、水谷誠、谷口貴実子、上田博章、古山政幸、石塚喜世伸、藤井寛、近本裕子、秋岡祐子、岡政史、野津寛大、飯島一誠、服部元史
- Organizer
  第45回日本小児腎臓病学会学術集会
- Place of Presentation
  大阪国際会議場(大阪府)
- Year and Date
  2010-07-02
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] The Relationship between Arginine Vasopressin Levels and Hyponatremia in Children Receiving Hypotonic or Isotonic Intravenous Fluids Following a Percutaneous Renal Biopsy2010
- Author(s)
  Michael L.Moritz,Nozu K, Iijima K
- Organizer
  Renal Week 2010
- Place of Presentation
  Colorado Convention Center(アメリカ)
- Year and Date
  2010-11-16
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] 常染色体劣性遺伝を呈したAlport症候群の一例2010
- Author(s)
  藤本陽子、古野由美、椛島成利、中俣潤一、坂東健一郎、柴田達哉、芹野良太、岡政史、飯島一誠、野津寛大、田村雅仁、尾辻豊
- Organizer
  第53回日本腎臓学会学術総会
- Place of Presentation
  神戸国際会議場(兵庫県)
- Year and Date
  2010-06-16
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] Clinical and Immunohistochemical Analyses of Japanese Families with Genetically-Defined Autosomal-Recessive Alport Syndrome2010
- Author(s)
  Iijima K, Oka M, Hashimura Y, Otsuka Y, Kaito H, Sado Y, Yan K, Nakanishi K, Yoshikawa N, Nagasako H, Nozu K, Matsuo M
- Organizer
  Renal Week 2010
- Place of Presentation
  Colorado Convention Center(アメリカ)
- Year and Date
  2010-11-16
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] 常染色体劣性多発性嚢胞腎(ARPKD)モデルcpkマウスの尿細管上皮細胞における上皮間葉移行(EMT)2010
- Author(s)
  戸川寛子、中西浩一、島友子、佐古まゆみ、向山弘展、宮嶋正康、野津寛大、吉原大輔、長尾枝澄香、飯島一誠、吉川徳茂
- Organizer
  第45回日本小児腎臓病学会学術集会
- Place of Presentation
  大阪国際会議場(大阪府)
- Year and Date
  2010-07-02
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] Natural Remission Rate and Prognostic Factors in Childhood IgANephropathy with Minimal Change or Focal Mesangial Proliferation2010
- Author(s)
  Shima Y,Nakanishi K,Togawa H,Nozu N,Tanaka T,Iijima K,Yoshikawa N
- Organizer
  the 15th Congress of the International Pediatric Nephrology Association
- Place of Presentation
  New York Hilton(アメリカ)
- Year and Date
  2010-08-29
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] Clinical and Immunohistochemical Analyses of Japanese Families with Genetically-Defined Autosomal-Recessive Alport Syndrome.2010
- Author(s)
  Iijima K, Oka M, Hashimura Y, Ohtsuka Y, Kaito H, Sado Y, Yan K, Nakanishi K, Yoshikawa N, Nagasako H, Nozu K, Matsuo M.
- Organizer
  American Society of Nephrology 2010 Annual Meeting
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] 平滑筋腫合併アルポート症候群(DL-AS)の遺伝学的検討2010
- Author(s)
  岡政史、野津寛大、森貞直哉、平野大志、藤永周一郎、忍頂寺毅史、橋村裕也、貝藤裕史、飯島一誠、松尾雅文
- Organizer
  第53回日本腎臓学会学術総会
- Place of Presentation
  神戸国際会議場(兵庫県)
- Year and Date
  2010-06-16
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] シクロスポリンにてネフローゼ症候群と食物アレルギー性腸炎の寛解維持が可能となったIPEX症候群の一例2010
- Author(s)
  野田俊輔、亀井宏一、堤晶子、宇田川智宏、小椋雅夫、伊藤秀一、松岡健太郎、金兼弘和、野津寛大、飯島一誠
- Organizer
  第45回日本小児腎臓病学会学術集会
- Place of Presentation
  大阪国際会議場(大阪府)
- Year and Date
  2010-07-02
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] Prognostic Factors in Childhood IgA Nephropathy with Focal Mesangial Proliferation Treated with Angiotensin Converting Enzyme Inhibitors2010
- Author(s)
  Shima Y, Nakanishi K, Togawa H, Mukaiyama H, Hama T, Nozu K, Tanaka R, Iijima K, Yoshikawa N
- Organizer
  Renal Week 2010
- Place of Presentation
  Colorado Convention Center(アメリカ)
- Year and Date
  2010-11-16
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] 常染色体性Alport症候群の臨床および分子生物学的検討2010
- Author(s)
  岡政史、野津寛大、忍頂寺毅史、橋村裕也、貝藤裕史、飯島一誠、松尾雅文
- Organizer
  第45回日本小児腎臓病学会学術集会
- Place of Presentation
  大阪国際会議場(大阪府)
- Year and Date
  2010-07-02
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] X染色体連鎖型Alport症候群の臨床的検討2010
- Author(s)
  橋村裕也、野津寛大、岡政史、忍頂寺毅史、貝藤裕史、飯島一誠、中西浩一、吉川徳茂、松尾雅文
- Organizer
  第53回日本腎臓学会学術総会
- Place of Presentation
  神戸国際会議場(兵庫県)
- Year and Date
  2010-06-16
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] 「CAKUTに対する治療戦略」CAKUTと遺伝子変異2010
- Author(s)
  飯島一誠, 野津寛大, 中山真紀子
- Organizer
  第32回日本小児腎不全学会学術集会
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] レシピエント選定基準改定後に経験した小児献腎移植の5例2010
- Author(s)
  忍頂寺毅史、橋村裕也、貝藤裕史、野津寛大、飯島一誠、松尾雅文
- Organizer
  第113回日本小児科学会学術集会
- Place of Presentation
  いわて県民情報交流センター(岩手県)
- Year and Date
  2010-04-25
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] LINE-1レトロトランスポゾンの置換によるEYA1遺伝子変異をともなったbranchio-oto-renal症候群の1女児例2010
- Author(s)
  森貞直哉、野津寛大、Nanna Dahl Rendtorff、森下高弘、宮川隆之、松元透、LisbethTrahebjaerg、飯島一誠、松尾雅文、楠原浩一
- Organizer
  第45回日本小児腎臓病学会学術集会
- Place of Presentation
  大阪国際会議場(大阪府)
- Year and Date
  2010-07-02
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] ヒトARPKDと相同遺伝子変異を有するPCK ratにおける上皮間葉移行2010
- Author(s)
  戸川寛子、中西浩一、島友子、佐古まゆみ、向山弘展、宮嶋正康、野津寛大、吉原大輔、長尾枝澄香、飯島一誠、吉川徳茂
- Organizer
  第53回日本腎臓学会学術総会
- Place of Presentation
  神戸国際会議場(兵庫県)
- Year and Date
  2010-06-16
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] Treatment Strategy and Outcome for Henoch-Schonlein Purpura Nephritis2010
- Author(s)
  Ninchoj T, Hashimura Y, Kaito H, Nozu N, Kanda, K, Kamioka I, Shima Y, Hamahira K, Nakanishi K, Tanaka R, Iijima K, Yoshikawa N, Matsuo M
- Organizer
  the 15th Congress of the International Pediatric Nephrology Association
- Place of Presentation
  New York Hilton(アメリカ)
- Year and Date
  2010-08-29
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] 常染色体劣性Alport症候群女児例におけるIV型コラーゲンα1～α6鎖染色の検討2010
- Author(s)
  三浦健一郎、高橋和浩、関根孝司、柳澤敦広、生井良幸、野津寛大、岡政史、飯島一誠、内藤一郎、五十嵐隆
- Organizer
  第113回日本小児科学会学術集会
- Place of Presentation
  いわて県民情報交流センター(岩手県)
- Year and Date
  2010-04-25
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] A Deep Intronic Mutation in the SLC12A3 Gene Leads to Gitelman Syndrome2009
- Author(s)
  Nozu K, Iijima K, Kaito H, Hashimura Y, Ninchoji T, Nakanishi K, Yoshikawa N, Matsuo M
- Organizer
  American Society of Nephrology 2009 Annual Meeting
- Place of Presentation
  San Diego Convention Center(America)
- Year and Date
  2009-10-30
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] 遺伝性腎疾患における intron 内の変異に伴う病気発症メカニズム解明のための実験系の確立2009
- Author(s)
  野津寛大, 貝藤裕史, 橋村裕也, 忍頂寺毅史, 飯島一誠, 松尾雅文, 中西浩一, 吉川徳茂
- Organizer
  第39回日本腎臓学会西部学術大会
- Place of Presentation
  和歌山県民文化会館(和歌山県)
- Year and Date
  2009-10-17
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] 等張性輸液は手術後の低ナトリウム(Na)血症を防止する2009
- Author(s)
  橋村裕也, 神田杏子, 野津寛大, 飯島一誠, 松尾雅文
- Organizer
  第52回日本腎臓学会学術総会
- Place of Presentation
  パシフィコ横浜(神奈川県)
- Year and Date
  2009-06-03
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] IPEX 症候群に微小変化型ネフローゼ症候群を合併した1症例2009
- Author(s)
  橋村裕也, 野津寛大, 神田杏子, 早川晶, 竹島泰弘, 飯島一誠, 松尾雅文, 中西浩一, 吉川徳茂
- Organizer
  第44回日本小児腎臓病学会学術集会
- Place of Presentation
  一橋記念講堂・学術総合センター(東京都)
- Year and Date
  2009-06-27
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] X染色体連鎖型アルポート症候群(XLAS)の分子遺伝学的検討2009
- Author(s)
  野津寛大, 貝藤裕史, 神田杏子, 橋村裕也, 飯島一誠, 松尾雅文, 中西浩一, 吉川徳茂
- Organizer
  第52回日本腎臓学会学術総会
- Place of Presentation
  パシフィコ横浜(神奈川県)
- Year and Date
  2009-06-05
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] Snail1 Is Involved in Epithelial-to-Mesenchymal Transition(EMT)in Cyst-Lining Epithelial Cells in PCK Rat2009
- Author(s)
  Togawa H, Nakanishi K, Shima Y, Sako M, Miyajima M, Nozu K, Iijima K, Yoshihara D, Nagao S, Yoshikawa N
- Organizer
  American Socrety of Nephrology 2009 Annual Meeting
- Place of Presentation
  San Diego Convention Center(America)
- Year and Date
  2009-10-29
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] Investigation of Molecular Background for Patients with Exercise-Induced Acute Renal Failure2009
- Author(s)
  Kaito H, Nozu K, Nakanishi K, Yoshikawa N, Iijima K, Matsuo M
- Organizer
  American Society of Nephrology 2009 Annual Meeting
- Place of Presentation
  San Diego Convention Center(America)
- Year and Date
  2009-10-31
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] 重症小児IgA腎症における治療反応性規定因子2009
- Author(s)
  島友子, 中西浩一, 戸川寛子, 尾鼻美奈, 野津寛大, 飯島一誠, 田中亮二郎, 佐々木聡, 吉川彼茂
- Organizer
  第44回日本小児腎臓病学会学術集会
- Place of Presentation
  一橋記念講堂・学術総合センター(東京都)
- Year and Date
  2009-06-27
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] 遺伝性腎疾患におけるintron内の変異に伴う病気発症メカニズム解明のためのin vivoおよびin vitroの実験系の確立2009
- Author(s)
  野津寛大
- Organizer
  第44回日本小児腎臓病学会学術集会
- Place of Presentation
  東京大学(東京都)
- Year and Date
  2009-06-27
- Data Source
  KAKENHI-PROJECT-21790986
[Presentation] 腎不全に至ったステロイド感受性微小変化型ネフローゼ症候群の1例2009
- Author(s)
  橋村裕也, 忍頂寺毅史, 貝藤裕史, 野津寛大, 飯島一誠, 中西浩一, 吉川徳茂, 松尾雅文
- Organizer
  第39回日本腎臓学会西部学術大会
- Place of Presentation
  和歌山県民文化会館(和歌山県)
- Year and Date
  2009-10-16
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] A Deep Intronic Mutation in the SLC12A3 Gene leads to Gitelman Syndrome.2009
- Author(s)
  Nozu K, Iijima K, Kaito H, Hashimura Y, Ninchoji T, Nakanishi K, Yoshikawa N, Matsuo M.
- Organizer
  American Society of Nephrology 2009 Annual Meeting
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] 遺伝性腎疾患における intron 内の変異に伴う病気発症メカニズム解明のための in vivo および in vitro の実験系の確立2009
- Author(s)
  野津寛大, 野津圭美, 齋木加代子, 西田篤丈, 貝藤裕史, 神田杏子, 橋村裕也, 中西浩一, 吉川徳茂, 河井和夫, 竹島泰弘, 飯島一誠, 松尾雅文
- Organizer
  第44回日本小児腎臓病学会学術集会
- Place of Presentation
  一橋記念講堂・学術総合センター(東京都)
- Year and Date
  2009-06-27
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] 小児ネフローゼ症候群患者におけるリツキシマブ血中濃度と投与後再発についての検討2009
- Author(s)
  貝藤裕史, 亀井宏一, 菊池絵梨子, 小椋雅夫, 佐古まゆみ, 野津寛大, 藤永秀一郎, 飯島一誠, 伊藤秀一
- Organizer
  第44回日本小児腎臓病学会学術集会
- Place of Presentation
  一橋記念講堂・学術総合センター(東京都)
- Year and Date
  2009-06-26
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] 運動後急性腎不全とPRES(Posterior reversible encephalopathy syndrome)の合併を反復した腎性低尿酸血症の1例2009
- Author(s)
  島友子, 中西浩一, 戸川寛子, 野津寛大, 飯島一誠, 吉川徳茂
- Organizer
  第39回日本腎臓学会西部学術大会
- Place of Presentation
  和歌山県民文化会館(和歌山県)
- Year and Date
  2009-10-16
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] NR3C2遺伝子変異に伴いmRNAに splicing 異常を認めたにも関わらず軽症であった偽性低アルドステロン症1型の親子例2009
- Author(s)
  神田杏子, 野津寛大, 橋村裕也, 三輪明弘, 森岡一朗, 横山直樹, 飯島一誠, 松尾雅文
- Organizer
  第44回日本小児腎臓病学会学術集会
- Place of Presentation
  一橋記念講堂・学術総合センター(東京都)
- Year and Date
  2009-06-27
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] ヒトARPKD相同遺伝子ラットモデルにおける尿細管部位特異的嚢胞形成2009
- Author(s)
  戸川寛子, 中西浩一, 島友子, 佐古まゆみ, 宮嶋正康, 野津寛大, 飯島一越, 吉原大輔, 長尾枝澄香, 吉川徳茂
- Organizer
  第52回日本腎臓学会学術総会
- Place of Presentation
  パシフィコ横浜(神奈川県)
- Year and Date
  2009-06-04
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] COL4A5遺伝子に9塩基の欠失を有し GBMに4型コラーゲンα5鎖の正常の発現を認めたX染色体連鎖型アルポート症候群男児例2009
- Author(s)
  沢登恵美, 海野杏奈, 金井宏明, 松下香子, 杉田完爾, 東田耕輔, 野津寛大, Rafal P Krol, 飯島一誠
- Organizer
  第44回日本小児腎臓病学会学術集会
- Place of Presentation
  一橋記念講堂・学術総合センター(東京都)
- Year and Date
  2009-06-27
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] X染色体連鎖型アルポート症候群の分子遺伝学的検討2009
- Author(s)
  野津寛大, Krol Rafal, 神田杏子, 橋村裕也, 中西浩一, 吉川徳茂, 飯島一誠, 松尾雅文
- Organizer
  第112回日本小児科学会学術集会
- Place of Presentation
  奈良県立文化会館(奈良県)
- Year and Date
  2009-04-17
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] X染色体連鎖型アルポート症候群の男性患者における糸球体基底膜4型コラーゲンα5鎖陽性例の検討2009
- Author(s)
  Krol R, Nozu K, Nakanishi K, Yoshikawa N, Iijima K, Matsuo M
- Organizer
  第44回日本小児腎臓病学会学術集会
- Place of Presentation
  一橋記念講堂・学術総合センター(東京都)
- Year and Date
  2009-06-26
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] ARPKD 相同遺伝子ラットモデルの尿細管上皮細胞における上皮間葉移行(EMT)2009
- Author(s)
  戸川寛子, 中酉浩一, 島友子, 佐古まゆみ, 宮嶋正康, 野津寛大, 飯島一誠, 吉原大輔, 長尾枝澄香, 吉川徳茂
- Organizer
  第44回日本小児腎臓病学会学術集会
- Place of Presentation
  一橋記念講堂・学術総合センター(東京都)
- Year and Date
  2009-06-27
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] 重症小児IgA腎症における治療後腎IgA沈着消失の臨床病理学的意義2009
- Author(s)
  島友子, 中西浩一, 戸川寛子, 尾鼻美奈, 野津寛大, 飯島一誠, 田中亮二郎, 佐々木聡, 吉川徳茂
- Organizer
  第52回日本腎臓学会学術総会
- Place of Presentation
  パシフィコ横浜(神奈川県)
- Year and Date
  2009-06-03
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] Disappearance of Glomerular IgA Deposits in Severe Childhood IgA Nephropathy after 2-yr Combination/Prednisolone Therapy.2008
- Author(s)
  Shima Y, Nakanishi K, Togawa H, Obana M, Nozu K, Tanaka R, Sasaki s, Iijima K, Yoshikawa N.
- Organizer
  American Society of Nephrology 2008 Annual Meeting
- Place of Presentation
  Philadelphia, USA
- Year and Date
  2008-11-07
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] Bartter症候群とGitelman症候群の病型と臨床症状2008
- Author(s)
  野津寛大
- Organizer
  第43回日本小児腎臓病学会学術集会
- Place of Presentation
  福岡
- Data Source
  KAKENHI-PROJECT-19790720
[Presentation] Epithelial-to-Mesenchymal Transition in Cyst-Lining Epithelial Cells in PCK Rat、2008
- Author(s)
  Togawa H, Nakanishi K, Obana M, Shima Y, Miyajima M, Nozu K, Iijima K, Nishi K, Nagao S, Takahashi H, Yoshikawa N.
- Organizer
  American Society of Nephrology 2008 Annual Meeting
- Place of Presentation
  Philadelphia, USA
- Year and Date
  2008-11-07
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] The First Case of Minimal Change Nephrotic Syndrome Associated with Immunodysregulation, Polyendocrinopathy, Enteropathy, X-Linked (IPEX) Syndrome2008
- Author(s)
  Hashimura Y, Nozu K, Kanda K, Takeshima Y, Hayakawa A, Iijima K, Matsuo M
- Organizer
  American Society of Nephrology 2008 Annual Meeting
- Place of Presentation
  Philadelphia, USA
- Year and Date
  2008-11-06
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] TCF2 Mutation in Patients with Congenital Anomalies of the Kidney and Urinary Tract (CAKUT).2008
- Author(s)
  Nakayama M, Nozu K, Goto Y, Kamei K, Sato H, Emi M, Iijima K.
- Organizer
  American Society of Nephrology 2008 Annual Meeting
- Place of Presentation
  Philadelphia, USA
- Year and Date
  2008-11-07
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] Somatic Mosaicism for a Mutation of the COL4A5 Gene in Three Sporadic X-Linked Alport Syndrome Cases.2008
- Author(s)
  Nozu K, Krol PR, Nakanishi K, Yoshikawa N, Kaito H, Kanda K, Hashimura Y, Iijima K, Matsuo M.
- Organizer
  American Society of Nephrology 2008 Annual Meeting
- Place of Presentation
  Philadelphia, USA
- Year and Date
  2008-11-08
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] The First Case of Minimal Change Nephrotic Syndrome Associated with Immunodysregulation, Polyendocrinopathy, Enteropathy, X-Linked (IPEX) Syndrome.2008
- Author(s)
  Hashimura Y, Nozu K, Kanda K, Takeshima Y, Hayakawa A, Iijima K, Matsuo M.
- Organizer
  American Society of Nephrology 2008 Annual Meeting
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] TCF2 Mutation in Patients with Congenital Anomalies of the Kidney and Urinary Tract (CAKUT).2008
- Author(s)
  Nakayama M, Nozu K, Goto Y, Kamei K, Sato H, Emi M, Iijima K
- Organizer
  American Society of Nephrology 2008 Annual Meeting
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] Elevated AVP Levels and Hyponatremia Following Percutaneous Renal Biopsies in Children.2008
- Author(s)
  Moritz ML, Iiiima K, Matsuo M, Kanda K, Nozu K.
- Organizer
  American Society of Nephrology 2008 Annual Meeting
- Place of Presentation
  Philadelphia, USA
- Year and Date
  2008-11-07
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] 運動後急性腎不全8症例におけるURATl遺伝子解析の検討.2008
- Author(s)
  貝藤裕史, 野津寛大, 飯島一誠, 中西浩一, 太田和秀, 藤枝幹也, 由良和夫, 亀井宏一, 横山忠史, 石原正行, 島友子, 神田杏子, 吉川徳茂, 松尾雅文
- Organizer
  第43回日本小児腎臓病学会学術集会
- Place of Presentation
  福岡
- Year and Date
  2008-06-13
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] Molecular analysis of 5 Japanese Patients with Type III Bartter Syndrome2008
- Author(s)
  Nozu K
- Organizer
  14th Congress of the International Pediatric Nephrology Association
- Place of Presentation
  Budapest, Hangury
- Year and Date
  2008-09-01
- Data Source
  KAKENHI-PROJECT-19790720
[Presentation] 先天性腎尿路奇形におけるTCF2遺伝子異常2008
- Author(s)
  中山真紀子, 後藤由紀, 亀井宏一, 野津寛大, 飯島一誠.
- Organizer
  第43回日本小児腎臓病学会学術集会
- Place of Presentation
  福岡
- Year and Date
  2008-06-14
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] IgA沈着が消失した重症型小児IgA腎症26例の検討2008
- Author(s)
  島友子, 中西浩一, 戸川寛子, 尾鼻美奈, 野津寛大, 田中亮二郎, 佐々木聡, 飯島一誠, 吉川徳茂.
- Organizer
  第43回日本小児腎臓病学会学術集会
- Place of Presentation
  福岡
- Year and Date
  2008-06-14
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] X染色体連鎖型アルポート症候群の分子遺伝学的検討.2008
- Author(s)
  野津寛大, KrolRafal, 貝藤裕史, 神田杏子, 橋村裕也, 松尾雅文, 中西浩一, 吉川徳茂, 飯島一誠.
- Organizer
  第43回日本小児腎臓病学会学術集会
- Place of Presentation
  福岡
- Year and Date
  2008-06-14
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] Bartter症候群、Gitelman症候群の病型と臨床症状2008
- Author(s)
  野津寛大
- Organizer
  第43回日本小児腎臓病学会学術集会
- Place of Presentation
  福岡
- Year and Date
  2008-06-13
- Data Source
  KAKENHI-PROJECT-19790720
[Presentation] 発端者のCOL4A5遺伝子に体細胞モザイクに変異を有し、軽症の臨床症状を示したAlport症候群の2家系.2008
- Author(s)
  野津寛大, 貝藤裕史, 神田杏子, 松尾雅文, 島友子, 戸川寛子, 中西浩一, 吉川徳茂, 飯島一誠.
- Organizer
  第43回日本小児腎臓病学会学術集会
- Place of Presentation
  福岡
- Year and Date
  2008-06-14
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] 小手術後の一過性血漿抗利尿ホルモン分泌亢進に関する研究.2008
- Author(s)
  神田杏子, 野津寛大, 貝藤裕史, 松尾雅文, 中西浩一, 吉川徳茂, 飯島一誠
- Organizer
  第51回日本腎臓学会学術総会
- Place of Presentation
  福岡
- Year and Date
  2008-05-31
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] Treatment of Refractory Steroid-Dependent Nephrotic Syndrome with a Single Dose of Rituximab, a Multicenter Prospective Study.2008
- Author(s)
  Kamei K, Nozu K, Ito S, Fujinaga S, Iijima K.
- Organizer
  American Society of Nephrology 2008 Annual Meeting
- Place of Presentation
  Philadelphia, USA
- Year and Date
  2008-11-07
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] III型Bartter症候群患者における利尿剤負荷試験 Gitelman症候群との類似性の機序に関する研究.2008
- Author(s)
  神田杏子, 野津寛大, 貝藤裕史, 松尾雅文, 亀井宏一, 飯島一誠, 中西浩一, 吉川徳茂, 関根孝司, 五十嵐隆, 小松博史, 宮下律子.
- Organizer
  第43回日本小児腎臓病学会学術集会
- Place of Presentation
  福岡
- Year and Date
  2008-06-14
- Data Source
  KAKENHI-PROJECT-20390240
[Presentation] Alport症候群：軽症患者における病理学的および分子生物学的検討
- Author(s)
  野津寛大
- Organizer
  第13回日本腎病理協会研究会
- Place of Presentation
  東京
- Year and Date
  2015-01-10 – 2015-01-11
- Invited
- Data Source
  KAKENHI-PROJECT-25893131
[Presentation] Autosomal Dominant Alport Syndrome: Molecular Analysis of the COL4A3/COL4A4 Genes and Clinical Outcome.
- Author(s)
  Kamiyoshi N, Nozu k, Matsunoshita N, Ohtsubo H, Ninchoji T, Kaito H, Nakanishi N, Yoshikawa N, Iijima K
- Organizer
  American Society of Nephrology Kidney Week 2014
- Place of Presentation
  Pennsylvania Convention Center (Philadelphia, USA)
- Year and Date
  2014-11-11 – 2014-11-16
- Data Source
  KAKENHI-PROJECT-26293203
[Presentation] X-linked Alport syndrome patients caused by atypical splicing mutations in COL4A5.
- Author(s)
  Nozu K, Morisada N, Kaito H, Ninchoji T, Nakanishi K, Yoshikawa N, Iijima K
- Organizer
  47th Annual Scientific Meeting of the European Society for Pediatric Nephrology
- Place of Presentation
  Alfandega Congress Center (Porta, Portugal)
- Year and Date
  2014-09-18 – 2014-09-20
- Data Source
  KAKENHI-PROJECT-26293203
[Presentation] X-linked Alport syndrome patients caused by atypical splicing mutations in COL4A5
- Author(s)
  Kandai Nozu, Naoya Morisada, Hiroshi Kaito, Takeshi Ninchoji, Koichi Nakanishi, Norishige Yoshikawa, Kazumoto Iijima
- Organizer
  Annual Meeting of the European Society for Pediatric Nephrology
- Place of Presentation
  Port
- Year and Date
  2014-09-18 – 2014-09-20
- Data Source
  KAKENHI-PROJECT-25893131
[Presentation] アルポート症候群-重症軽症を規定する因子に関する再考
- Author(s)
  野津寛大
- Organizer
  第49回日本小児腎臓病学会学術集会
- Place of Presentation
  秋田
- Year and Date
  2014-06-05 – 2014-06-07
- Invited
- Data Source
  KAKENHI-PROJECT-25893131
[Presentation] Alport syndrome
- Author(s)
  Kandai Nozu
- Organizer
  The 12th Japan-Korea Pediatric Nephrology Seminar
- Place of Presentation
  Kobe
- Year and Date
  2014-04-19 – 2014-04-20
- Invited
- Data Source
  KAKENHI-PROJECT-25893131

1. IIJIMA Kazumoto (00240854)

# of Collaborated Projects: 10 results

# of Collaborated Products: 226 results
2. 堀之内智子 (30754593)

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5. NAKAYAMA Makioko (80469999)

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6. NAGATA Michio (10192238)

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7. MORISADA Naoya (00389446)

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8. HASHIMURA Yuya (80457077)

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9. NISHIO Hisahide (80189258)

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10. MATSUO Masafumi (10157266)

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13. NISHIYAMA Kaoru (00150061)

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14. SIRAKAWA Taku (30171044)

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15. Yamamura Tomohiko (30770242)

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16. MINAMIKAWA Shogo (10772634)

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22. 石森真吾 (30465950)

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23. 榊原菜々 (90814319)

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24. 薗田啓之 (60970853)

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25. NAKANISHI Koichi

# of Collaborated Projects: 0 results

# of Collaborated Products: 21 results
26. SHIMA Yuko

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# of Collaborated Products: 18 results
27. SHIINA Masaaki

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# of Collaborated Products: 1 results
28. YOSHIKAWA Norishige

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29. TANAKA Hiroshi

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30. USUI Joichi

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31. 緒方一博

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32. 首藤剛

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34. 吉田瑶子

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NODU KANDAI 野津 寛大

KANDAI Nozu 野津 寛大

NOZU Kandai 野津 寛大

野津 寛大 ノヅ カンダイ

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Contribution of aberrant splicing to the onset mechanisms in inherited kidney diseasesPrincipal Investigator

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Contribution of aberrant splicing to the onset mechanisms in inherited kidney diseasesPrincipal Investigator

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The onset mechanisms for inherited salt-losing tubulopathiesPrincipal Investigator

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Nonsense read-through therapy for Aport syndromePrincipal Investigator

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最新の遺伝子解析技術を駆使した先天性尿細管チャネル・輸送体異常症の分子機構の解明Principal Investigator

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NODU KANDAI 野津寛大

KANDAI Nozu 野津寛大

NOZU Kandai 野津寛大

野津寛大ノヅカンダイ

[Book] Alport症候群の軽症亜型　Annual Review 2015腎臓2015

[Journal Article] 【遺伝を考える】(II章)遺伝学的診断　個別診療分野における遺伝学的診断の進歩　腎・泌尿器領域2023

[Journal Article] 【遺伝を考える】(II章)遺伝学的診断　個別診療分野における遺伝学的診断の進歩　腎・泌尿器領域2023